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Name |
Telatinib |
EINECS | N/A |
CAS No. | 332012-40-5 | Density | 1.418 g/cm3 |
PSA | 102.17000 | LogP | 4.41730 |
Solubility | N/A | Melting Point |
N/A |
Formula | C20H16ClN5O3 | Boiling Point | 713.595 °C at 760 mmHg |
Molecular Weight | 409.832 | Flash Point | 385.368 °C |
Transport Information | N/A | Appearance | N/A |
Safety | Risk Codes | N/A | |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
Bay57-9352;Telatinib [INN];4-[[4-(4-Chloroanilino)furo[2,3-d]pyridazin-7-yl]oxymethyl]-N-methylpyridine-2-carboxamide;BAY-579352;2-Pyridinecarboxamide,4-[[[4-[(4-chlorophenyl)amino]furo[2,3-d]pyridazin-7-yl]oxy]methyl]-N-methyl-;UNII-18P7197Q7J; |
Article Data | 4 |
4-(hydroxymethyl)-N-methylpyridine-2-carboxamide
4-chloroanilino-7-chlorofuro[2,3-d]pyridazine
Telatinib
Conditions | Yield |
---|---|
With potassium hydroxide; 18-crown-6 ether In toluene at 83 - 87℃; Product distribution / selectivity; | 46% |
With potassium hydroxide; 18-crown-6 ether In toluene at 20 - 85℃; | 46% |
4-(hydroxymethyl)-N-methylpyridine-2-carboxamide
4-chloro-7-[N-(4-chlorophenyl)amino]-[2,3-d]furopyridazine
Telatinib
Conditions | Yield |
---|---|
With potassium hydroxide; 18-crown-6 ether In toluene at 20 - 87℃; Product distribution / selectivity; | 46% |
Stage #1: 4-(hydroxymethyl)-N-methylpyridine-2-carboxamide; 4-chloro-7-[N-(4-chlorophenyl)amino]-[2,3-d]furopyridazine; 18-crown-6 ether In toluene at 20℃; for 0.166667h; Stage #2: With potassium hydroxide In toluene at 80℃; for 24h; Product distribution / selectivity; |
4-chloroanilino-7-chlorofuro[2,3-d]pyridazine
2-methylaminocarbonyl-4-pyridylcarbinol hydrochloride
Telatinib
Conditions | Yield |
---|---|
With potassium tert-butylate In tetrahydrofuran; toluene at 95℃; for 24h; Temperature; Time; Autoclave; | 37.7% |
N-Methylformamide
A
Telatinib
B
4-(4-chlorophenylamino)-2-methylaminocarbonyl-7-(2-methylaminocarbonyl-4-pyridylmethoxy)-furo[2,3-d]pyridazine
Conditions | Yield |
---|---|
With sulfuric acid; hydroxylamine-O-sulfonic acid; iron(II) sulfate In water at 20℃; for 1.83333h; Product distribution / selectivity; | A 15.2% B n/a |
Stage #1: N-Methylformamide; N-(4-chlorophenyl)-7-(4-pyridinylmethoxy)-furo[2,3-d]pyridazin-4-amine With sulfuric acid; iron(II) sulfate; hydroxylamine-O-sulfonic acid In water at 20℃; for 1.83333h; Stage #2: With sodium citrate In water at 0℃; for 0.166667h; Product distribution / selectivity; | A 15.2% B n/a |
With sulfuric acid; iron(II) sulfate; hydroxylamine-O-sulfonic acid In water at 20℃; for 1.66667h; | A 15.2% B n/a |
ethyl 2-methylaminocarbonyl-4-picolinate
Telatinib
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: sodium tetrahydroborate / isopropyl alcohol; methanol / 8 h / 25 °C / Large scale 1.2: 1 h / 0 °C / Large scale 2.1: potassium tert-butylate / toluene; tetrahydrofuran / 24 h / 95 °C / Autoclave View Scheme | |
Multi-step reaction with 2 steps 1.1: sodium tetrahydroborate / ethanol / 18 h / 20 °C 1.3: pH 9 2.1: potassium hydroxide; 18-crown-6 ether / toluene / 83 - 87 °C View Scheme | |
Multi-step reaction with 2 steps 1: sodium tetrahydroborate / ethanol / 18 h / 20 °C 2: potassium hydroxide; 18-crown-6 ether / toluene / 20 - 85 °C View Scheme |
4,7-dichlorofuro[2,3-d]pyridazine
Telatinib
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: ethanol / 4 h / Heating / reflux 2: potassium hydroxide; 18-crown-6 ether / toluene / 83 - 87 °C View Scheme | |
Multi-step reaction with 2 steps 1: ethanol / 4 h / Heating / reflux 2: potassium hydroxide; 18-crown-6 ether / toluene / 20 - 85 °C View Scheme |
4,7-dichlorofuro[2,3-d]pyridazine
A
Telatinib
B
4-(4-chlorophenylamino)-2-methylaminocarbonyl-7-(2-methylaminocarbonyl-4-pyridylmethoxy)-furo[2,3-d]pyridazine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: ethanol / 4 h / Heating / reflux 2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / 24 h / 125 °C 3.1: sulfuric acid; iron(II) sulfate; hydroxylamine-O-sulfonic acid / water / 1.83 h / 20 °C 3.2: 0.17 h / 0 °C View Scheme | |
Multi-step reaction with 3 steps 1: ethanol / 4 h / Heating / reflux 2: 1,8-diazabicyclo[5.4.0]undec-7-ene / 24 h / 125 °C 3: sulfuric acid; iron(II) sulfate; hydroxylamine-O-sulfonic acid / water / 1.67 h / 20 °C View Scheme |
isonicotinic acid ethylester
Telatinib
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: sulfuric acid; dihydrogen peroxide; iron(II) sulfate / water / 0.5 h / 6 - 22 °C 1.2: pH ~ 5 2.1: sodium tetrahydroborate / ethanol / 18 h / 20 °C 2.3: pH 9 3.1: potassium hydroxide; 18-crown-6 ether / toluene / 83 - 87 °C View Scheme | |
Multi-step reaction with 3 steps 1: sulfuric acid; dihydrogen peroxide; iron(II) sulfate / water / 0.5 h / 6 - 22 °C 2: sodium tetrahydroborate / ethanol / 18 h / 20 °C 3: potassium hydroxide; 18-crown-6 ether / toluene / 20 - 85 °C View Scheme |
furan-2,3-dicarboxylic acid
Telatinib
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: chloro-trimethyl-silane / 15.5 h / 20 °C 2.1: ethanol; water; hydrazine / 5.5 h / Heating / reflux 2.2: 4 h / Heating / reflux 3.1: pyridine; trichlorophosphate / 4 h / Heating / reflux 4.1: ethanol / 4 h / Heating / reflux 5.1: potassium hydroxide; 18-crown-6 ether / toluene / 83 - 87 °C View Scheme | |
Multi-step reaction with 5 steps 1: chloro-trimethyl-silane / 15.5 h / 20 °C 2: hydrazine / ethanol / 5.5 h / Heating / reflux 3: pyridine; trichlorophosphate / 4 h / Heating / reflux 4: ethanol / 4 h / Heating / reflux 5: potassium hydroxide; 18-crown-6 ether / toluene / 20 - 85 °C View Scheme |
furan-2,3-dicarboxylic acid
A
Telatinib
B
4-(4-chlorophenylamino)-2-methylaminocarbonyl-7-(2-methylaminocarbonyl-4-pyridylmethoxy)-furo[2,3-d]pyridazine
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: chloro-trimethyl-silane / 15.5 h / 20 °C 2.1: ethanol; water; hydrazine / 5.5 h / Heating / reflux 2.2: 4 h / Heating / reflux 3.1: pyridine; trichlorophosphate / 4 h / Heating / reflux 4.1: ethanol / 4 h / Heating / reflux 5.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / 24 h / 125 °C 6.1: sulfuric acid; iron(II) sulfate; hydroxylamine-O-sulfonic acid / water / 1.83 h / 20 °C 6.2: 0.17 h / 0 °C View Scheme | |
Multi-step reaction with 6 steps 1: chloro-trimethyl-silane / 15.5 h / 20 °C 2: hydrazine / ethanol / 5.5 h / Heating / reflux 3: pyridine; trichlorophosphate / 4 h / Heating / reflux 4: ethanol / 4 h / Heating / reflux 5: 1,8-diazabicyclo[5.4.0]undec-7-ene / 24 h / 125 °C 6: sulfuric acid; iron(II) sulfate; hydroxylamine-O-sulfonic acid / water / 1.67 h / 20 °C View Scheme |
IUPAC Name: [(8Z,12Z,14E)-6-Hydroxy-5,11-dimethoxy-3,7,9,15-tetramethyl-16,20,22-trioxo-21-(prop-2-enylamino)-17-azabicyclo[16.3.1]docosa-1(21),8,12, 14,18-pentaen-10-yl] carbamate
Molecular Formula: C31H43N3O8
Molecular Weight: 585.69g/mol
Density: 1.21
Melting Point: 201-203°C
The Cas Register Number of Telatinib is 75747-14-7 .The chemical synonyms of Telatinib (CAS NO. 75747-14-7) are Geldanamycin,17-demethoxy-17-(2-propenylamino)- ; CP 127374 ; Allylaminogeldanamycin ; 17-(Allylamino)-17-demethoxygeldanamycin ; 17-(Allylamino)-17-desmethoxygeldanamycin ; 17-(Allylamino)-17-dimethoxygeldanamycin ; 17-Allylaminogeldanamycin ; 17-AG .The molecular structure of Telatinib (CAS NO. 75747-14-7) is.
It is a substance that is being studied in the treatment of cancer, specific young patients with certain types of leukemia or solid tumors, especially kidney tumors.
Hazard Codes:Xi
Risk Statements: 36/37/38
R36: Irritating to eyes.
R37: Irritating to respiratory system
R38: Irritating to skin.
Safety Statements: 22-24/25-36-26
S22: Do not breathe dust.
S24/25: Avoid contact with skin and eyes.
S36: Wear suitable protective clothing.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany: 3
The extinguishing agent of Telatinib (CAS NO. 75747-14-7) are dry powder, foam, sand, carbon dioxide, water mist.