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Large Stock 99.0% 4-Benzylpiperidine 31252-42-3 Producer
Cas No: 31252-42-3
USD $ 0.1-0.1 / Gram 1 Gram 100 Metric Ton/Year Xi'an Xszo Chem Co., Ltd. Contact Supplier
?4-Benzylpiperidine
Cas No: 31252-42-3
No Data 10 Milligram Amadis Chemical Co., Ltd. Contact Supplier
4-Benzylpiperidine
Cas No: 31252-42-3
No Data No Data No Data Chemwill Asia Co., Ltd. Contact Supplier
4-Benzylpiperidine
Cas No: 31252-42-3
USD $ 3.0-3.0 / Kilogram 1 Kilogram 1-100 Metric Ton/Month Dayang Chem (Hangzhou) Co.,Ltd. Contact Supplier
CAS No.31252-42-3 4-BENZYLPIPERIDINE
Cas No: 31252-42-3
No Data 1 Liter 5000 Liter/Year Henan Tianfu Chemical Co., Ltd. Contact Supplier
Manufacturer supply CAS 31252-42-3 with best quality
Cas No: 31252-42-3
USD $ 139.0-210.0 / Kilogram 1 Kilogram 1000 Kilogram/Day Zhuozhou Wenxi import and Export Co., Ltd Contact Supplier
Piperidine,4-(phenylmethyl)- 31252-42-3
Cas No: 31252-42-3
No Data 1 Kilogram 10000 Metric Ton/Month Shanghai Upbio Tech Co.,Ltd Contact Supplier
Piperidine,4-(phenylmethyl)-
Cas No: 31252-42-3
No Data 1 Kilogram 1 Metric Ton/Day Shandong Hanjiang Chemical Co., Ltd. Contact Supplier
Guaranteed Quality with Bulk Price CAS 31252-42-3 4-BENZYLPIPERIDINE
Cas No: 31252-42-3
USD $ 30.0-50.0 / Kilogram 25 Kilogram 1000 Kilogram/Week Wuhan Alpha & Omega Pharmaceuticals Co., Ltd Contact Supplier
4-BENZYLPIPERIDINE
Cas No: 31252-42-3
No Data 1 Gram 1000 Gram/Week Shanghai BetterBioChem Co., Ltd. Contact Supplier

31252-42-3 Usage

Chemical Properties

CLEAR COLOURLESS TO YELLOW VISCOUS LIQUID

Synthesis Reference(s)

Synthesis, p. 741, 1980 DOI: 10.1055/s-1980-29196

Uses

Reactant for synthesis of:? ;Antiproliferatives1? ;GABA uptake inhibitors2? ;Pyridines3? ;Histamine H3 antagonists4? ;Multipotent drugs with cholinergic and neuroprotective properties for the treatment of Alzheimers and neuronal vascular diseases5 ? ;Antiserotoninergic, antiplatelet, hemorheologic, antiarrythmic and antioxidant molecules via nucleophilic substitution6

Uses

4-Benzylpiperidine was studied as acid corrosion inhibitor for iron. 4-Benzylpiperidine was also used to study potential utility of dopamine-welective releaser as a treatment for cocaine dependence. In an assay of cocaine discrimination, 4-?Benzylpiperidine had the most rapid onset and shortest duration of action.
InChI:InChI=1/C12H17N/c1-2-4-11(5-3-1)10-12-6-8-13-9-7-12/h1-5,12-13H,6-10H2/p+1

31252-42-3 Well-known Company Product Price

Brand (Code)Product description CAS number Packaging Price Detail
Alfa Aesar (B23883)  4-Benzylpiperidine, 98%    31252-42-3 25g 414.0CNY Detail
Alfa Aesar (B23883)  4-Benzylpiperidine, 98%    31252-42-3 100g 1146.0CNY Detail
Alfa Aesar (B23883)  4-Benzylpiperidine, 98%    31252-42-3 500g 4862.0CNY Detail
Aldrich (142360)  4-Benzylpiperidine  99% 31252-42-3 142360-25G 341.64CNY Detail

31252-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BENZYLPIPERIDINE

1.2 Other means of identification

Product number -
Other names 4-Benzyl-piperidine

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:31252-42-3 SDS

31252-42-3Synthetic route

4-benzyl-1-[(4-methylphenyl)sulfonyl]piperidine
205641-99-2

4-benzyl-1-[(4-methylphenyl)sulfonyl]piperidine

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
Stage #1: 4-benzyl-1-[(4-methylphenyl)sulfonyl]piperidine With Na/K absorbed into silica gel In tetrahydrofuran at 20℃; Inert atmosphere;
Stage #2: With water In tetrahydrofuran
96%
92%
With dimethyl(phenyl)silyl lithium In tetrahydrofuran at 0℃;78%
piperidine
110-89-4

piperidine

benzaldehyde
100-52-7

benzaldehyde

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
With sodium tetrahydroborate; cetyltrimethylammonim bromide at 20℃; for 14h;96%
4-benzyl-N-tritylpiperidine
544478-05-9

4-benzyl-N-tritylpiperidine

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
Stage #1: 4-benzyl-N-tritylpiperidine With naphthalene; lithium In tetrahydrofuran at 0℃; for 1h;
Stage #2: With water In tetrahydrofuran at 0 - 20℃;
91%
1-nitroso-4-(phenylmethyl)piperidine
15104-07-1

1-nitroso-4-(phenylmethyl)piperidine

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
With sodium tetrahydroborate; titanium tetrachloride In 1,2-dimethoxyethane for 14h; Ambient temperature;90%
With sodium tetrahydroborate; nickel dichloride In tetrahydrofuran for 6h; Ambient temperature;90%
4-benzyl-N-(triphenylsilyl)piperidine

4-benzyl-N-(triphenylsilyl)piperidine

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
With naphthalene; lithium In tetrahydrofuran; methanol at 20℃; for 5h;89%
4-benzyl-1-(methanesulfonyl)piperidine
132251-82-2

4-benzyl-1-(methanesulfonyl)piperidine

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
Stage #1: 4-benzyl-1-(methanesulfonyl)piperidine With Na/K absorbed into silica gel In tetrahydrofuran at 20℃; Inert atmosphere;
Stage #2: With water In tetrahydrofuran
89%
Product distribution / selectivity;83%
4-benzyl pyridine
2116-65-6

4-benzyl pyridine

A

4-Cyclohexylmethyl-piperidine
78197-28-1

4-Cyclohexylmethyl-piperidine

B

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
With hydrogenchloride; platinum Hydrogenation;
4-benzyl pyridine
2116-65-6

4-benzyl pyridine

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
With ethanol; sodium
With acetic acid; platinum Hydrogenation;
With nickel at 100℃; under 110326 - 220652 Torr; Hydrogenation;
With platinum(IV) oxide; hydrogen In acetic acid at 20℃; under 2585.81 Torr; for 12h;
Stage #1: 4-benzyl pyridine With hydrogen; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In octane at 120℃; under 15001.5 Torr; for 40h;
Stage #2: With water Catalytic behavior; chemoselective reaction;
> 99 %Chromat.
4-benzyl pyridine
2116-65-6

4-benzyl pyridine

ethanol
64-17-5

ethanol

sodium

sodium

A

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

B

4-benzyl-piperideine

4-benzyl-piperideine

1-(4-benzylpiperidin-1-yl)-2,2-dimethylpropan-1-one

1-(4-benzylpiperidin-1-yl)-2,2-dimethylpropan-1-one

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
With naphthalene; lithium In tetrahydrofuran at 0℃; for 1h;95 % Chromat.
4-bromopyridin
1120-87-2

4-bromopyridin

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1,3-bis[(diphenylphosphino)propane]dichloronickel(II) / tetrahydrofuran / 15 h / 20 °C
2: platinum(IV) oxide; hydrogen / acetic acid / 12 h / 20 °C / 2585.81 Torr
View Scheme
3-((4-benzylpiperidin-1-yl)methyl)-N,N-diethylaniline

3-((4-benzylpiperidin-1-yl)methyl)-N,N-diethylaniline

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Conditions
ConditionsYield
With acetic acid In water-d2 for 0.25h; Solvent; Irradiation;96 %Spectr.
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

trifluoroacetic acid
76-05-1

trifluoroacetic acid

Wang resin-linked N1-tert-butyloxycarbonyl-N2-triflylguanidine

Wang resin-linked N1-tert-butyloxycarbonyl-N2-triflylguanidine

4-benzyl-piperidine-1-carboxamidine; compound with trifluoro-acetic acid

4-benzyl-piperidine-1-carboxamidine; compound with trifluoro-acetic acid

Conditions
ConditionsYield
Stage #1: 4-benzylpyperidine; Wang resin-linked N1-tert-butyloxycarbonyl-N2-triflylguanidine In dichloromethane at 20℃;
Stage #2: trifluoroacetic acid In dichloromethane Further stages.;
100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

epichlorohydrin
106-89-8

epichlorohydrin

1-chloro-3-(4-benzylpiperidin-1-yl)propan-2-ol
438634-79-8

1-chloro-3-(4-benzylpiperidin-1-yl)propan-2-ol

Conditions
ConditionsYield
100%
In ethanol for 3h;
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

trifluoroacetic anhydride
407-25-0

trifluoroacetic anhydride

1-(trifluoroacetyl)-4-benzylpiperidine
157338-47-1

1-(trifluoroacetyl)-4-benzylpiperidine

Conditions
ConditionsYield
In dichloromethane at 20℃;100%
In ethyl acetate at 20℃; for 3h;97%
In dichloromethane88%
In dichloromethane at 20℃; for 1.5h;
In dichloromethane for 0.5h;
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

acetic anhydride
108-24-7

acetic anhydride

1-(4-benzylpiperidin-1-yl)ethan-1-one
101997-42-6

1-(4-benzylpiperidin-1-yl)ethan-1-one

Conditions
ConditionsYield
at 20℃; for 1h;100%
2-bromo-N-(1,3-dibromo-6-oxo-5,6-dihydro-4H-cyclopenta[c]thien-4-yl)acetamide
872408-08-7

2-bromo-N-(1,3-dibromo-6-oxo-5,6-dihydro-4H-cyclopenta[c]thien-4-yl)acetamide

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

2-(4-benzyl-piperidin-1-yl)-N-(1,3-dibromo-6-oxo-5,6-dihydro-4H-cyclopenta[c]thiophen-4-yl)-acetamide

2-(4-benzyl-piperidin-1-yl)-N-(1,3-dibromo-6-oxo-5,6-dihydro-4H-cyclopenta[c]thiophen-4-yl)-acetamide

Conditions
ConditionsYield
With potassium carbonate at 20℃; for 12h;100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

2-chloro-6-fluorobenzaldehyde
387-45-1

2-chloro-6-fluorobenzaldehyde

2-chloro-6-(4-benzylpiperidine)benzaldehyde
793706-92-0

2-chloro-6-(4-benzylpiperidine)benzaldehyde

Conditions
ConditionsYield
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 130℃; for 3.5h;100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Benzyl bromoacetate
5437-45-6

Benzyl bromoacetate

(4-benzylpiperidin-1-yl)acetic acid benzyl ester
438634-63-0

(4-benzylpiperidin-1-yl)acetic acid benzyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane; ethyl acetate100%
formaldehyd
50-00-0

formaldehyd

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

(4-nitrophenyl)ethanone
100-19-6

(4-nitrophenyl)ethanone

C34H41N3O3
1037020-24-8

C34H41N3O3

Conditions
ConditionsYield
With hydrogenchloride In ethanol Mannich reaction; Heating;100%
formaldehyd
50-00-0

formaldehyd

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

1-(4-methoxyphenyl)ethanone
100-06-1

1-(4-methoxyphenyl)ethanone

C35H44N2O2
1037020-22-6

C35H44N2O2

Conditions
ConditionsYield
With hydrogenchloride In ethanol Mannich reaction; Heating;100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

S-(3-phenylpropyl) 4-(p-tolyl)benzenecarbothioate
1178916-74-9

S-(3-phenylpropyl) 4-(p-tolyl)benzenecarbothioate

(4-benzyl-1-piperidyl)-[4-(p-tolyl)phenyl]methanone
1178916-75-0

(4-benzyl-1-piperidyl)-[4-(p-tolyl)phenyl]methanone

Conditions
ConditionsYield
With potassium phosphate; silver trifluoromethanesulfonate In acetonitrile at 70℃; for 16h;100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

benzaldehyde
100-52-7

benzaldehyde

N-benzyl-4-benzylpiperidine

N-benzyl-4-benzylpiperidine

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride In 2-methyltetrahydrofuran at 18℃; for 1h; Solvent; Reagent/catalyst; Green chemistry;100%
3-phenyl-propionaldehyde
104-53-0

3-phenyl-propionaldehyde

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

4-benzyl-1-(3-phenylpropyl)piperidine

4-benzyl-1-(3-phenylpropyl)piperidine

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride In 2-methyltetrahydrofuran at 18℃; for 1h; Solvent; Reagent/catalyst; Green chemistry;100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

(E)-4-(4-isopropylphenyl)-4-oxo-2-butenoic acid phenylamide
1220094-90-5

(E)-4-(4-isopropylphenyl)-4-oxo-2-butenoic acid phenylamide

2-(4-benzylpiperidinyl)-4-(4-isopropylphenyl)-4-oxo-N-phenylbutanamide

2-(4-benzylpiperidinyl)-4-(4-isopropylphenyl)-4-oxo-N-phenylbutanamide

Conditions
ConditionsYield
In dichloromethane; toluene Michael Addition;100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

3,4-dichloro-1,2,5-thiadiazole
5728-20-1

3,4-dichloro-1,2,5-thiadiazole

3-(4-benzylpiperidin-1-yl)-4-chloro-1,2,5-thiadiazole

3-(4-benzylpiperidin-1-yl)-4-chloro-1,2,5-thiadiazole

Conditions
ConditionsYield
at 110 - 120℃;100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

p-Toluic acid
99-94-5

p-Toluic acid

(4-benzylpiperidin-1-yl)(p-tolyl)methanone

(4-benzylpiperidin-1-yl)(p-tolyl)methanone

Conditions
ConditionsYield
Stage #1: p-Toluic acid With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate at 20℃; for 0.166667h;
Stage #2: 4-benzylpyperidine at 20℃; for 1h;
100%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

Ethyl oxalyl chloride
4755-77-5

Ethyl oxalyl chloride

(4-benzylpiperidin-1-yl)-oxoacetic acid ethyl ester
349119-55-7

(4-benzylpiperidin-1-yl)-oxoacetic acid ethyl ester

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 0.5h;99%
With TEA In chloroform at 10℃; for 2h;
With N-ethyl-N,N-diisopropylamine In dichloromethane15.5 g (99%)
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

toluene-4-sulfonic acid Chroman-3-ylmethyl ester
113771-46-3

toluene-4-sulfonic acid Chroman-3-ylmethyl ester

4-benzyl-1-chroman-3-ylmethyl-piperidine

4-benzyl-1-chroman-3-ylmethyl-piperidine

Conditions
ConditionsYield
In toluene for 12h; Heating;99%
formaldehyd
50-00-0

formaldehyd

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

4-benzyl-1-methylpiperidine
1557-31-9

4-benzyl-1-methylpiperidine

Conditions
ConditionsYield
With formic acid at 0 - 20℃; for 16h; Reflux;98%
With formic acid
With formic acid for 18h; Heating;
With formic acid In water for 24h; Reflux;
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

ortho-nitrofluorobenzene
1493-27-2

ortho-nitrofluorobenzene

4-benzyl-1-(2-nitro-phenyl)piperidine
455260-04-5

4-benzyl-1-(2-nitro-phenyl)piperidine

Conditions
ConditionsYield
Stage #1: 4-benzylpyperidine With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 1h;
Stage #2: ortho-nitrofluorobenzene In N,N-dimethyl-formamide at 0 - 20℃; Further stages.;
98%
formaldehyd
50-00-0

formaldehyd

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

potassium (benzo[b]thiophene-2-yl)trifluoroborate

potassium (benzo[b]thiophene-2-yl)trifluoroborate

1-benzo[b]thiophen-2-ylmethyl-4-benzyl-piperidine

1-benzo[b]thiophen-2-ylmethyl-4-benzyl-piperidine

Conditions
ConditionsYield
Stage #1: formaldehyd; 4-benzylpyperidine In toluene at 90℃;
Stage #2: potassium (benzo[b]thiophene-2-yl)trifluoroborate With boron trifluoride diethyl etherate In toluene at 90℃; for 5h; Further stages.;
98%
C12H15NO3S2

C12H15NO3S2

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

C24H32N2O3S2
865432-96-8

C24H32N2O3S2

Conditions
ConditionsYield
In dichloromethane98%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

C16H15ClOS
1178916-14-7

C16H15ClOS

(4-benzylpiperidin-1-yl)(4-chlorophenyl)methanone

(4-benzylpiperidin-1-yl)(4-chlorophenyl)methanone

Conditions
ConditionsYield
With potassium phosphate; silver trifluoromethanesulfonate In acetonitrile at 70℃; for 16h;98%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

3-acetyl-2-chloropyridine
55676-21-6

3-acetyl-2-chloropyridine

1-[2-(4-benzylpiperidin-1-yl)pyridin-3-yl]ethanone
1260147-79-2

1-[2-(4-benzylpiperidin-1-yl)pyridin-3-yl]ethanone

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 200℃; under 12929 Torr; for 0.25h; Microwave irradiation;98%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

N-(2-methoxybenzyl)-6-(4-phenylpiperidin-1-yl)-N-(pyridin-2-ylmethyl)hexan-1-amine
1258447-85-6

N-(2-methoxybenzyl)-6-(4-phenylpiperidin-1-yl)-N-(pyridin-2-ylmethyl)hexan-1-amine

6-(4-benzylpiperidin-1-yl)-N-(2-methoxybenzyl)-N-(pyridin-2-ylmethyl)hexan-1-amine
1258447-87-8

6-(4-benzylpiperidin-1-yl)-N-(2-methoxybenzyl)-N-(pyridin-2-ylmethyl)hexan-1-amine

Conditions
ConditionsYield
98%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

4-fluorophenyl N-[5-[(tert-butyldimethylsilyl)oxy]pyridin-2-yl]carbamate

4-fluorophenyl N-[5-[(tert-butyldimethylsilyl)oxy]pyridin-2-yl]carbamate

4-benzyl-N-[5-[(tert-butyldimethylsilyl)oxy]pyridin-2-yl]piperidine-1-carboxamide

4-benzyl-N-[5-[(tert-butyldimethylsilyl)oxy]pyridin-2-yl]piperidine-1-carboxamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 2h;98%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

1-t-butyloxycarbonyl-4-benzylpiperidine
251107-37-6

1-t-butyloxycarbonyl-4-benzylpiperidine

Conditions
ConditionsYield
With citric acid In tetrahydrofuran; ethyl acetate97.9%
With citric acid In tetrahydrofuran; ethyl acetate97.9%
In tetrahydrofuran for 20h; Heating / reflux;91%
formaldehyd
50-00-0

formaldehyd

4-benzylpyperidine
31252-42-3

4-benzylpyperidine

11-methylene-6,11-dihydrodibenzoxepin-2-acetic acid methyl ester
113836-34-3

11-methylene-6,11-dihydrodibenzoxepin-2-acetic acid methyl ester

{11-[2-(4-Benzyl-piperidin-1-yl)-eth-(E)-ylidene]-6,11-dihydro-dibenzo[b,e]oxepin-2-yl}-acetic acid methyl ester

{11-[2-(4-Benzyl-piperidin-1-yl)-eth-(E)-ylidene]-6,11-dihydro-dibenzo[b,e]oxepin-2-yl}-acetic acid methyl ester

Conditions
ConditionsYield
With acetic acid; trifluoroacetic acid In dichloromethane97%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

methyl thioisocyanate
556-61-6

methyl thioisocyanate

4-benzyl-piperidine-1-carbothioic acid methylamide

4-benzyl-piperidine-1-carbothioic acid methylamide

Conditions
ConditionsYield
In dichloromethane at 20℃; for 0.333333h; Addition;97%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

(4-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-yl)-dimethyl-amine
461670-34-8

(4-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-yl)-dimethyl-amine

4-(4-benzyl-1-piperidinyl)-6-dimethylamino-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine

4-(4-benzyl-1-piperidinyl)-6-dimethylamino-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine

Conditions
ConditionsYield
In tetrahydrofuran Heating;97%
4-benzylpyperidine
31252-42-3

4-benzylpyperidine

(S)-2-((tert-butoxycarbonyl)(methyl)amino)-3-(4-hydroxyphenyl)propanoic acid
82038-34-4

(S)-2-((tert-butoxycarbonyl)(methyl)amino)-3-(4-hydroxyphenyl)propanoic acid

1-[(S)-N-tert-butyloxycarbonyl-N-methyltyrosyl]-4-benzylpiperidine
516473-08-8

1-[(S)-N-tert-butyloxycarbonyl-N-methyltyrosyl]-4-benzylpiperidine

Conditions
ConditionsYield
With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In N,N-dimethyl-formamide at 20℃; for 24h;97%

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