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ChemicalBook--->CAS DataBase List--->920966-03-6

920966-03-6

920966-03-6 Structure

920966-03-6 Structure
IdentificationBack Directory
[Name]

1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 4-chloro-
[CAS]

920966-03-6
[Synonyms]

4-Chloro-7-azaindole-5-ca...
4-Chloro-7-azaindole-5-carboxylic acid
4-Chloro-7-azaindole-5-carboxylicacid95%
4-Chloro-7-azaindole-5-carboxylic acid 95%
4-Chloro-1H-pyrrol[2,3-b] pyridine-5-carboxylic acid
1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 4-chloro-
4-Chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid 95%
4-Chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid, 5-Carboxy-4-chloro-1H-pyrrolo[2,3-b]pyridine
[Molecular Formula]

C8H5ClN2O2
[MDL Number]

MFCD10574983
[MOL File]

920966-03-6.mol
[Molecular Weight]

196.59
Chemical PropertiesBack Directory
[density ]

1.644±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

solid
[pka]

0.70±0.30(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C8H5ClN2O2/c9-6-4-1-2-10-7(4)11-3-5(6)8(12)13/h1-3H,(H,10,11)(H,12,13)
[InChIKey]

SJZMFAGWKZNYPX-UHFFFAOYSA-N
[SMILES]

C12NC=CC1=C(Cl)C(C(O)=O)=CN=2
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 4-chloro-(920966-03-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

ethyl 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylate

885500-55-0

1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 4-chloro-

920966-03-6

General procedure for the synthesis of 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid from ethyl 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylate: to a solution of 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid ethyl ester (10.5 g, 46.7 mmol) in ethanol (84 mL), was added an aqueous 1 M sodium hydroxide solution ( 140 mL, 140 mmol) and the reaction mixture was stirred at 60 °C for 1.5 hours. Upon completion of the reaction, the mixture was cooled to 4 °C and acidified with 1 M aqueous hydrochloric acid to pH < 7. The precipitated solid was collected by filtration and washed with deionized water to afford 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid (9.0 g, 98% yield). The structure of the product was confirmed by 1H-NMR (DMSO-d6) δ: 6.62-6.64 (1H, m), 7.67-7.70 (1H, m), 8.71 (1H, s), 12.32 (1H, br s), 13.22 (1H, br s) and mass spectra (ESI) m/z: 195 (M-H)-.

[References]

[1] Chemical and Pharmaceutical Bulletin, 2015, vol. 63, # 5, p. 341 - 353
[2] Patent: WO2007/7919, 2007, A2. Location in patent: Page/Page column 45
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