ChemicalBook--->CAS DataBase List--->76006-11-6

76006-11-6

76006-11-6 Structure

76006-11-6 Structure
IdentificationBack Directory
[Name]

7-CHLORO-1H-PYRAZOLO[3,4-C]PYRIDINE
[CAS]

76006-11-6
[Synonyms]

76006-11-6
o[3,4-c]pyridine
7-chloro-1H-pyrazolo[3
7-CHLORO-1H-PYRAZOLO[3,4-C]PYRIDINE
1H-Pyrazolo[3,4-c]pyridine, 7-chloro-
7-Chloro-1H-pyrazolo[3,4-c]pyridine 97%
[Molecular Formula]

C6H4ClN3
[MDL Number]

MFCD09265710
[MOL File]

76006-11-6.mol
[Molecular Weight]

153.572
Chemical PropertiesBack Directory
[Melting point ]

161-163℃
[Boiling point ]

357.5±22.0 °C(Predicted)
[density ]

1.531
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

8.87±0.40(Predicted)
[Appearance]

Light yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H315-H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2933399990
Questions And AnswerBack Directory
[Application]

7-Chloro-1H-pyrazolo[3,4-C]pyridine can be used as an organic synthesis intermediate and a pharmaceutical intermediate, mainly in laboratory research and development and chemical production processes.
Spectrum DetailBack Directory
[Spectrum Detail]

7-CHLORO-1H-PYRAZOLO[3,4-C]PYRIDINE(76006-11-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Amino-2-chloro-4-methylpyridine

133627-45-9

7-CHLORO-1H-PYRAZOLO[3,4-C]PYRIDINE

76006-11-6

Step 1: A solution of sodium nitrite (7.36 g, 107 mmol) in water (30 mL) was slowly added dropwise to a solution of 2-chloro-3-amino-4-methylpyridine (10.14 g, 71.1 mmol) and potassium acetate (9.02 g, 92 mmol) in acetic acid (200 mL) while keeping the internal temperature below 13 °C. After the dropwise addition was completed, the reaction mixture was allowed to slowly warm to room temperature and stirred continuously for 66 hours. Upon completion of the reaction, the mixture was concentrated under reduced pressure and the residue was alkalized with saturated sodium bicarbonate solution. Subsequently, the solid product was collected by filtration and washed with distilled water. The resulting solid was stirred in ethyl acetate overnight and filtered again. The filtrate was combined with the organic extract, evaporated to dryness and adsorbed on silica gel, and purified by fast column chromatography (using 120 g silica gel, eluent ethyl acetate: hexane, gradient from 0:1 to 1:1), resulting in a white crystalline solid product, 7-chloro-1H-pyrazolo[3,4-c]pyridine (4.99 g, 46% yield). Mass spectrometry analysis showed m/z = 153.9, 155.9 [M + H]+, which corresponds to the theoretically calculated value of molecular weight 153 for C6H4ClN3.

[References]

[1] Patent: US2014/249104, 2014, A1. Location in patent: Page/Page column
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980, p. 2398 - 2404
[3] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980, p. 2398 - 2404
[4] Patent: WO2012/93101, 2012, A1. Location in patent: Page/Page column 154
[5] Patent: WO2014/2052, 2014, A1. Location in patent: Page/Page column 51
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