ChemicalBook--->CAS DataBase List--->74976-31-1

74976-31-1

74976-31-1 Structure

74976-31-1 Structure
IdentificationBack Directory
[Name]

6-CHLORO-5-AZAINDOLE
[CAS]

74976-31-1
[Synonyms]

6-CHORO-5-AZAINDOLE
6-Chloro-5-azaindol
6-CHLORO-5-AZAINDOLE
6-Chloro-1H-pyrrolo[3,2-c]pyridine
1H-Pyrrolo[3,2-c]pyridine, 6-chloro-
[Molecular Formula]

C7H5ClN2
[MDL Number]

MFCD08690133
[MOL File]

74976-31-1.mol
[Molecular Weight]

152.581
Chemical PropertiesBack Directory
[Melting point ]

193-194 °C(Solv: benzene (71-43-2))
[Boiling point ]

335.8±22.0 °C(Predicted)
[density ]

1.425±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

solid
[pka]

14.30±0.40(Predicted)
[color ]

Beige
[InChI]

InChI=1S/C7H5ClN2/c8-7-3-6-5(4-10-7)1-2-9-6/h1-4,9H
[InChIKey]

CBHXTZKXDLDMJZ-UHFFFAOYSA-N
[SMILES]

C1=NC(Cl)=CC2NC=CC1=2
[CAS DataBase Reference]

74976-31-1
Safety DataBack Directory
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

6-Chloro-5-azaindole is used in preparation of oxodiphenyldihydropyrazolecarboxamide derivatives and analogs for use as ACSS2 inhibitors.
[Synthesis]

4-Pyridinamine, 2-chloro-5-[(1E)-2-ethoxyethenyl]-

1190862-36-2

6-CHLORO-5-AZAINDOLE

74976-31-1

2-Chloro-5-[(E)-2-ethoxyvinyl]pyridin-4-amine (CAS:1190862-36-2, 1.00 g, 5.30 mmol) was used as a raw material, which was dissolved in methanol (20 mL), followed by the addition of concentrated hydrochloric acid (1.00 mL, 32.64 mmol). The reaction mixture was stirred at 75°C for 21 hours. Upon completion of the reaction, the mixture was concentrated under reduced pressure, neutralized with saturated aqueous potassium carbonate solution and then extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give 6-chloro-5-azaindole (0.76 g, 99% yield) as a beige solid. The product was detected by mass spectrometry (LRMS), m/z: 153 (M + 1)+; 1H-NMR (CDCl3) δ: 6.65 (m, 1H), 7.20 (s, 2H), 8.60 (m, 2H).

[References]

[1] Patent: EP2108641, 2009, A1. Location in patent: Page/Page column 49-50
Spectrum DetailBack Directory
[Spectrum Detail]

6-CHLORO-5-AZAINDOLE(74976-31-1)1HNMR
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