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918516-27-5

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918516-27-5 Usage

General Description

1H-Pyrrolo[2,3-b]pyridine, 5-(4-chlorophenyl)- is a chemical compound with the molecular formula C14H9ClN2. It is a heterocyclic aromatic compound that contains a pyrrole ring fused to a pyridine ring, with a 4-chlorophenyl substituent at the 5-position. 1H-Pyrrolo[2,3-b]pyridine, 5-(4-chlorophenyl)- is primarily used as a building block in the synthesis of various pharmaceuticals and biologically active molecules. It may also have potential applications in medicinal and agrochemical research due to its pharmacological properties. Additionally, it is important to handle this compound with care as it may have certain hazards and risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 918516-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,5,1 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 918516-27:
(8*9)+(7*1)+(6*8)+(5*5)+(4*1)+(3*6)+(2*2)+(1*7)=185
185 % 10 = 5
So 918516-27-5 is a valid CAS Registry Number.

918516-27-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 1H-Pyrrolo[2,3-b]pyridine,5-(4-chlorophenyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:918516-27-5 SDS

918516-27-5Synthetic route

4-Chlorophenylboronic acid
1679-18-1

4-Chlorophenylboronic acid

5-bromo-1H-pyrrolo[2,3-b]pyridine
183208-35-7

5-bromo-1H-pyrrolo[2,3-b]pyridine

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In Dimethyl ether; water Solvent; Temperature; Reflux;92%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,2-dimethoxyethane; water Reflux;92%
With bis-triphenylphosphine-palladium(II) chloride; potassium carbonate In 1,2-dimethoxyethane at 130℃; for 0.5h; Suzuki coupling; Inert atmosphere; Microwave irradiation;76%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With sodium hydroxide In water; N,N-dimethyl-formamide at 100℃; for 10h;81.3%
5-(4-Cl-phenyl)azaindole
1356397-48-2

5-(4-Cl-phenyl)azaindole

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With potassium tert-butylate In 1-methyl-pyrrolidin-2-one at 20 - 120℃; for 2h; Product distribution / selectivity;80%
With potassium tert-butylate In 1-methyl-pyrrolidin-2-one at 20 - 120℃; for 2h;
5-chloro-1H-pyrrolo[2,3-b]pyridine
866546-07-8

5-chloro-1H-pyrrolo[2,3-b]pyridine

phenylboronic acid
98-80-6

phenylboronic acid

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate; caesium carbonate In water; toluene Inert atmosphere; Reflux;75%
C14H9ClN2O2
1431663-20-5

C14H9ClN2O2

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With quinoline; copper chromite at 220℃; for 0.2h; Microwave irradiation;58%
2-azido-3-(5-(4-chlorophenyl)pyridine-3-yl)acrylic acid

2-azido-3-(5-(4-chlorophenyl)pyridine-3-yl)acrylic acid

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With quinoline; copper chromite at 220℃; for 0.2h; Microwave irradiation;43%
5-bromo-2-pyridylamine
1072-97-5

5-bromo-2-pyridylamine

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium diacetate / 1,4-dioxane; water / 1.5 h / 90 °C
2: trifluoroacetic acid; N-iodo-succinimide / N,N-dimethyl-formamide / 2.5 h / 80 °C
3: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C / Inert atmosphere
4: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
Multi-step reaction with 4 steps
1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium diacetate / 1,4-dioxane; water / 1.5 h / 90 °C
2: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C
3: N,N,N',N'-tetramethylguanidine; copper(l) iodide / bis-triphenylphosphine-palladium(II) chloride / toluene / 2 h / 100 °C / Inert atmosphere
4: potassium tert-butylate / 1-methyl-pyrrolidin-2-one / 2 h / 20 - 120 °C
View Scheme
Multi-step reaction with 4 steps
1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium diacetate / 1,4-dioxane; water / 1.5 h / 90 °C
2: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C
3: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C
4: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
4-Chlorophenylboronic acid
1679-18-1

4-Chlorophenylboronic acid

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium diacetate / 1,4-dioxane; water / 1.5 h / 90 °C
2: trifluoroacetic acid; N-iodo-succinimide / N,N-dimethyl-formamide / 2.5 h / 80 °C
3: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C / Inert atmosphere
4: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
Multi-step reaction with 4 steps
1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium diacetate / 1,4-dioxane; water / 1.5 h / 90 °C
2: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C
3: N,N,N',N'-tetramethylguanidine; copper(l) iodide / bis-triphenylphosphine-palladium(II) chloride / toluene / 2 h / 100 °C / Inert atmosphere
4: potassium tert-butylate / 1-methyl-pyrrolidin-2-one / 2 h / 20 - 120 °C
View Scheme
Multi-step reaction with 4 steps
1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium diacetate / 1,4-dioxane; water / 1.5 h / 90 °C
2: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C
3: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C
4: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
5-(4-chlorophenyl)pyridin-2-ylamine
84596-08-7

5-(4-chlorophenyl)pyridin-2-ylamine

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: trifluoroacetic acid; N-iodo-succinimide / N,N-dimethyl-formamide / 2.5 h / 80 °C
2: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C / Inert atmosphere
3: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
Multi-step reaction with 3 steps
1: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C
2: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C
3: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
Multi-step reaction with 3 steps
1: trifluoroacetic acid; N-iodo-succinimide / N,N-dimethyl-formamide / 2.5 h / 80 °C
2: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane; water / 24 h / 80 °C
3: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
C11H8BrClN2
911113-60-5

C11H8BrClN2

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C
2: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1: N,N,N',N'-tetramethylguanidine; copper(l) iodide / bis-triphenylphosphine-palladium(II) chloride / toluene / 2 h / 100 °C / Inert atmosphere
2: potassium tert-butylate / 1-methyl-pyrrolidin-2-one / 2 h / 20 - 120 °C
View Scheme
Multi-step reaction with 2 steps
1: N,N,N',N'-tetramethylguanidine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / toluene / 2 h / 100 °C / Inert atmosphere
2: potassium tert-butylate / 1-methyl-pyrrolidin-2-one / 2 h / 20 - 120 °C
View Scheme
Multi-step reaction with 2 steps
1: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C
2: hydrogenchloride / N,N-dimethyl-formamide; water / 1 h / 50 °C
View Scheme
C15H15ClN2O
1356397-47-1

C15H15ClN2O

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With hydrogenchloride In water at 50℃; for 1h; Product distribution / selectivity; Inert atmosphere;
With hydrogenchloride In water; N,N-dimethyl-formamide at 50℃; for 1h;
C11H8ClIN2
1356397-46-0

C11H8ClIN2

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C / Inert atmosphere
2: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane; water / 24 h / 80 °C
2: hydrogenchloride / water / 1 h / 50 °C / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C / Inert atmosphere
2: hydrogenchloride / N,N-dimethyl-formamide; water / 1 h / 50 °C
View Scheme
Multi-step reaction with 2 steps
1: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane; water / 24 h / 80 °C
2: hydrogenchloride / N,N-dimethyl-formamide; water / 1 h / 50 °C
View Scheme
C11H9ClN2*(x)ClH

C11H9ClN2*(x)ClH

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: sodium hydroxide / water
2: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C
3: N,N,N',N'-tetramethylguanidine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / toluene / 2 h / 100 °C / Inert atmosphere
4: potassium tert-butylate / 1-methyl-pyrrolidin-2-one / 2 h / 20 - 120 °C
View Scheme
Multi-step reaction with 4 steps
1: sodium hydroxide / water
2: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C
3: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C
4: hydrogenchloride / N,N-dimethyl-formamide; water / 1 h / 50 °C
View Scheme
Multi-step reaction with 4 steps
1: sodium hydroxide / water
2: trifluoroacetic acid; N-iodo-succinimide / N,N-dimethyl-formamide / 2.5 h / 80 °C
3: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / N,N-dimethyl-formamide / 18 h / 70 °C / Inert atmosphere
4: hydrogenchloride / N,N-dimethyl-formamide; water / 1 h / 50 °C
View Scheme
Multi-step reaction with 4 steps
1: sodium hydroxide / water
2: trifluoroacetic acid; N-iodo-succinimide / N,N-dimethyl-formamide / 2.5 h / 80 °C
3: lithium hydroxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane; water / 24 h / 80 °C
4: hydrogenchloride / N,N-dimethyl-formamide; water / 1 h / 50 °C
View Scheme
C15H11ClN4O2

C15H11ClN4O2

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: lithium hydroxide / tetrahydrofuran
2: quinoline; copper chromite / 0.2 h / 220 °C / Microwave irradiation
View Scheme
Multi-step reaction with 3 steps
1: toluene / 0.2 h / 200 °C / Microwave irradiation
2: lithium hydroxide / tetrahydrofuran
3: quinoline; copper chromite / 0.2 h / 220 °C / Microwave irradiation
View Scheme
methyl 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylate
1426575-26-9

methyl 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylate

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: lithium hydroxide / tetrahydrofuran
2: quinoline; copper chromite / 0.2 h / 220 °C / Microwave irradiation
View Scheme
4-chlorophenylboronic acid pinacol ester
195062-61-4

4-chlorophenylboronic acid pinacol ester

5-bromo-1H-pyrrolo[2,3-b]pyridine
183208-35-7

5-bromo-1H-pyrrolo[2,3-b]pyridine

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With sodium carbonate In water at 120℃; for 0.5h; Irradiation;19 mg
bromochlorobenzene
106-39-8

bromochlorobenzene

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: potassium acetate; tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane / 0.75 h / 120 °C / Irradiation
2: sodium carbonate / water / 0.5 h / 120 °C / Irradiation
View Scheme
5-bromo-1-(tert-butyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile
1372929-27-5

5-bromo-1-(tert-butyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; sodium carbonate / toluene; water / 7 h / 85 °C / Inert atmosphere
2: aluminum (III) chloride / chlorobenzene / 100 °C / Inert atmosphere
3: hydrogen bromide; water / 24 h / 100 °C
4: sodium hydroxide / water; dimethyl sulfoxide / 24 h / 113 - 115 °C
View Scheme
5-(4-chlorophenyl)-1-(tert-butyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile
1418299-52-1

5-(4-chlorophenyl)-1-(tert-butyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: aluminum (III) chloride / chlorobenzene / 100 °C / Inert atmosphere
2: hydrogen bromide; water / 24 h / 100 °C
3: sodium hydroxide / water; dimethyl sulfoxide / 24 h / 113 - 115 °C
View Scheme
4-chlorophenylacetic Acid
1878-66-6

4-chlorophenylacetic Acid

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1.1: trichlorophosphate / 8 h / 70 °C
1.2: 2 h / 10 - 26 °C
2.1: sodium methylate / methanol; dimethyl sulfoxide / 1 h / 100 °C / Inert atmosphere
3.1: aluminum (III) chloride / chlorobenzene / 100 °C / Inert atmosphere
4.1: hydrogen bromide; water / 24 h / 100 °C
5.1: sodium hydroxide / water; dimethyl sulfoxide / 24 h / 113 - 115 °C
View Scheme
Multi-step reaction with 5 steps
1.1: trichlorophosphate / 2.75 h / 10 - 85 °C / Inert atmosphere
1.2: 1.5 h / 0 - 5 °C
2.1: caesium carbonate / dimethyl sulfoxide / 1.5 h / 80 °C / Inert atmosphere
3.1: aluminum (III) chloride / chlorobenzene / 100 °C / Inert atmosphere
4.1: hydrogen bromide; water / 24 h / 100 °C
5.1: sodium hydroxide / water; dimethyl sulfoxide / 24 h / 113 - 115 °C
View Scheme
N-(2-(4-chlorophenyl)-3-(dimethylamino)allylidene)-N-methylmethanaminium hexafluorophosphate

N-(2-(4-chlorophenyl)-3-(dimethylamino)allylidene)-N-methylmethanaminium hexafluorophosphate

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: sodium methylate / methanol; dimethyl sulfoxide / 1 h / 100 °C / Inert atmosphere
2: aluminum (III) chloride / chlorobenzene / 100 °C / Inert atmosphere
3: hydrogen bromide; water / 24 h / 100 °C
4: sodium hydroxide / water; dimethyl sulfoxide / 24 h / 113 - 115 °C
View Scheme
N-(2-(4-chlorophenyl)-3-(dimethylamino)allylidene)-N-methylmethanaminium tetrafluoroborate

N-(2-(4-chlorophenyl)-3-(dimethylamino)allylidene)-N-methylmethanaminium tetrafluoroborate

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: caesium carbonate / dimethyl sulfoxide / 1.5 h / 80 °C / Inert atmosphere
2: aluminum (III) chloride / chlorobenzene / 100 °C / Inert atmosphere
3: hydrogen bromide; water / 24 h / 100 °C
4: sodium hydroxide / water; dimethyl sulfoxide / 24 h / 113 - 115 °C
View Scheme
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: hydrogen bromide; water / 24 h / 100 °C
2: sodium hydroxide / water; dimethyl sulfoxide / 24 h / 113 - 115 °C
View Scheme
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid hydrobromide

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid hydrobromide

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With sodium hydroxide In water; dimethyl sulfoxide at 113 - 115℃; for 24h;31.8 g
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2,6-difluoro-3-(propane-1-sulfonylamino)benzoic acid
1103234-56-5

2,6-difluoro-3-(propane-1-sulfonylamino)benzoic acid

vemurafenib

vemurafenib

Conditions
ConditionsYield
Stage #1: 2,6-difluoro-3-(propane-1-sulfonylamino)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 2.5h;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine; aluminum (III) chloride In dichloromethane at 20℃; for 3h;
85%
Stage #1: 2,6-difluoro-3-(propane-1-sulfonylamino)benzoic acid With oxalyl dichloride In dichloromethane at 18 - 26℃; for 2h;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane at 0 - 26℃; for 5h;
70%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2-methyl-5-(propylsulfonamido)benzoic acid

2-methyl-5-(propylsulfonamido)benzoic acid

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-4-methylphenyl)propane-1-sulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-4-methylphenyl)propane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 2-methyl-5-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride
80%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

benzoyl chloride
98-88-4

benzoyl chloride

C20H13ClN2O
1426575-27-0

C20H13ClN2O

Conditions
ConditionsYield
With zirconium(IV) chloride Friedel-Crafts Acylation;79%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2-fluoro-5-(propylsulfonamido)benzoic acid
918524-58-0

2-fluoro-5-(propylsulfonamido)benzoic acid

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-4-fluorophenyl)propane-1-sulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-4-fluorophenyl)propane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 2-fluoro-5-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride
71%
Stage #1: 2-fluoro-5-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane Friedel-Crafts Acylation;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane Friedel-Crafts Acylation;
71%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2-fluoro-3-(propylsulfonamido)benzoic acid
918523-49-6

2-fluoro-3-(propylsulfonamido)benzoic acid

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-fluorophenyl)propane-1-sulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-fluorophenyl)propane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 2-fluoro-3-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride
68%
Stage #1: 2-fluoro-3-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane Friedel-Crafts Acylation;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane Friedel-Crafts Acylation;
68%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

N-(2,4-difluoro-3-formylphenyl)propane-1-sulfonamide
918523-58-7

N-(2,4-difluoro-3-formylphenyl)propane-1-sulfonamide

N-(3-(bis(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)methyl)-2,4-difluorophenyl)propane-1-sulfonamide
1522361-91-6

N-(3-(bis(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)methyl)-2,4-difluorophenyl)propane-1-sulfonamide

Conditions
ConditionsYield
With potassium carbonate In methanol; water at 130℃; for 0.5h; Microwave irradiation;64%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2,6-difluoro-3-(propylsulfonamido)benzoyl chloride
1186194-32-0

2,6-difluoro-3-(propylsulfonamido)benzoyl chloride

vemurafenib

vemurafenib

Conditions
ConditionsYield
Stage #1: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In 1,2-dichloro-ethane at 0℃; for 0.666667h;
Stage #2: 2,6-difluoro-3-(propylsulfonamido)benzoyl chloride In 1,2-dichloro-ethane at 0 - 20℃;
60%
With aluminum (III) chloride In dichloromethane at 0 - 20℃; for 3h;
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2,6-difluoro-3-(2-methylpropylsulfonamido)benzoic acid
1186194-09-1

2,6-difluoro-3-(2-methylpropylsulfonamido)benzoic acid

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)-2-methylpropane-1-sulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)-2-methylpropane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine; 2,6-difluoro-3-(2-methylpropylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane
Stage #2: With aluminum (III) chloride In dichloromethane
58%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

3-fluoro-5-(propylsulfonamido)benzoic acid

3-fluoro-5-(propylsulfonamido)benzoic acid

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-5-fluorophenyl)propane-1-sulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-5-fluorophenyl)propane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 3-fluoro-5-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane Friedel-Crafts Acylation;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane Friedel-Crafts Acylation;
55%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2,6-difluoro-3-(pentylsulfonamido)benzoic acid

2,6-difluoro-3-(pentylsulfonamido)benzoic acid

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)pentane-1-sulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)pentane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 2,6-difluoro-3-(pentylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride
54%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2-methyl-3-(propylsulfonamido)benzoic acid

2-methyl-3-(propylsulfonamido)benzoic acid

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-methylphenyl)propane-1-sulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-methylphenyl)propane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 2-methyl-3-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride
53%
Stage #1: 2-methyl-3-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane Friedel-Crafts Acylation;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane Friedel-Crafts Acylation;
53%
3-(propylsulfonamido)benzoic acid
849409-82-1

3-(propylsulfonamido)benzoic acid

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)phenyl)-propane-1-sulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)phenyl)-propane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 3-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane Friedel-Crafts Acylation;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane Friedel-Crafts Acylation;
52%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2-chloro-3-(propylsulfonamido)benzoic acid

2-chloro-3-(propylsulfonamido)benzoic acid

N-(2-chloro-3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)phenyl)propane-1-sulfonamide

N-(2-chloro-3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)phenyl)propane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 2-chloro-3-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride
46%
Stage #1: 2-chloro-3-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane Friedel-Crafts Acylation;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane Friedel-Crafts Acylation;
46%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

acetyl chloride
75-36-5

acetyl chloride

1-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone

1-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone

Conditions
ConditionsYield
Stage #1: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane at 20℃; for 0.5h;
Stage #2: acetyl chloride In dichloromethane at 20℃; for 12h;
Stage #3: With sodium hydroxide In water pH=5;
42%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

C10H11BrClNO3S

C10H11BrClNO3S

N-(3-bromo-5-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)phenyl)propane-1-sulfonamide

N-(3-bromo-5-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)phenyl)propane-1-sulfonamide

Conditions
ConditionsYield
With aluminum (III) chloride In dichloromethane at 20℃;38%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

C12H13F2NO3

C12H13F2NO3

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)butyramide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)butyramide

Conditions
ConditionsYield
Stage #1: C12H13F2NO3 With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane at 20℃;
38%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

4-fluoro-3-(propylsulfonamido)benzoic acid

4-fluoro-3-(propylsulfonamido)benzoic acid

N-(5-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-fluorophenyl)propane-1-sulfonamide

N-(5-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2-fluorophenyl)propane-1-sulfonamide

Conditions
ConditionsYield
Stage #1: 4-fluoro-3-(propylsulfonamido)benzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane Friedel-Crafts Acylation;
Stage #2: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine With aluminum (III) chloride In dichloromethane Friedel-Crafts Acylation;
37%
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

2,6-difluoro-3-(ethylsulfonamido)benzoic acid
1186609-71-1

2,6-difluoro-3-(ethylsulfonamido)benzoic acid

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)ethanesulfonamide

N-(3-(5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)ethanesulfonamide

Conditions
ConditionsYield
With aluminum (III) chloride; oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane29%
methanol
67-56-1

methanol

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
918516-27-5

5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

N-(2,4-difluoro-3-formylphenyl)propane-1-sulfonamide
918523-58-7

N-(2,4-difluoro-3-formylphenyl)propane-1-sulfonamide

A

propane-1-sulfonic acid (3-{[5-(4-chloro-phenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-methoxy-methyl}-2,4-difluoro-phenyl)-amide

propane-1-sulfonic acid (3-{[5-(4-chloro-phenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-methoxy-methyl}-2,4-difluoro-phenyl)-amide

B

propane-1-sulfonic acid (3-{[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-yl]hydroxymethyl}-2,4-difluorophenyl)amide

propane-1-sulfonic acid (3-{[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-yl]hydroxymethyl}-2,4-difluorophenyl)amide

Conditions
ConditionsYield
With potassium hydroxide at 20℃; for 72h;
With potassium hydroxide at 20℃; for 72h;

918516-27-5Relevant articles and documents

PROTEIN KINASE INHIBITORS FOR PROMOTING LIVER REGENERATION OR REDUCING OR PREVENTING HEPATOCYTE DEATH

-

Page/Page column 46; 47, (2020/02/14)

The invention relates to compounds of formula (I) which are inhibitors of MKK4 (mitogen-activated protein kinase kinase 4) and their use in promoting liver regeneration or reducing or preventing hepatocyte death. The compounds selectively inhibit protein kinase MKK4 over protein kinases JNK and MKK7. (I), wherein R x, R y , R z and R zz are selected from: a) R x and R y are F and R z and R zz are H; b) R x, R y and R zz are independently halogen and R z is H; c) R x R z and R zz are independently halogen and R y is H; and d) R x R y and R z are independently halogen and R zz is H

Synthesis of novel 7-azaindole derivatives containing pyridin-3-ylmethyl dithiocarbamate moiety as potent PKM2 activators and PKM2 nucleus translocation inhibitors

Liu, Bin,Yuan, Xia,Xu, Bo,Zhang, Han,Li, Ridong,Wang, Xin,Ge, Zemei,Li, Runtao

, p. 1 - 15 (2019/03/17)

Multiple lines of evidence have indicated that pyruvate kinase M2 (PKM2) is upregulated in most cancer cells and it is increasingly recognized as a potential therapeutic target in oncology. In a continuation of our discovery of lead compound 5 and SAR study, the 7-azaindole moiety in compound 5 was systematically optimized. The results showed that compound 6f, which has a difluoroethyl substitution on the 7-azaindole ring, exhibited high PKM2 activation potency and anti-proliferation activities on A375 cell lines. In a xenograft mouse model, oral administration of compound 6f led to significant tumor regression without obvious toxicity. Further mechanistic studies revealed that 6f could influence the translocation of PKM2 into nucleus, as well as induction of apoptosis and autophagy of A375 cells. More importantly, compound 6f significantly inhibited migration of A375 cells in a concentration-dependent manner. Collectively, 6f may serve as a lead compound in the development of potent PKM2 activators for cancer therapy.

PROTEIN KINASE INHIBITORS FOR PROMOTING LIVER REGENERATION OR REDUCING OR PREVENTING HEPATOCYTE DEATH

-

Page/Page column 35; 36; 79; 80, (2018/08/12)

The invention relates to MKK4 (mitogen-activated protein kinase 4) and their use in promoting liver regeneration or reducing or preventing hepatocyte death. The MKK4 inhibitors selectively inhibit protein kinase MKK4 over protein kinases JNK and MKK7.

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