ChemicalBook--->CAS DataBase List--->1187190-69-7

1187190-69-7

1187190-69-7 Structure

1187190-69-7 Structure
IdentificationBack Directory
[Name]

6-Chloro-4-methoxypyridine-3-carbonitrile
[CAS]

1187190-69-7
[Synonyms]

6-chloro-4-Methoxynicotinonitrile
6-Chloro-4-methoxypyridine-3-carbonitrile
3-Pyridinecarbonitrile, 6-chloro-4-methoxy-
6-Chloro-4-Methoxy-Nicotinonitrile(WX683504)
6-Chloro-4-Methoxy-Nicotinonitrile Achiral 73.43
[Molecular Formula]

C7H5ClN2O
[MDL Number]

MFCD16250655
[MOL File]

1187190-69-7.mol
[Molecular Weight]

168.58
Chemical PropertiesBack Directory
[storage temp. ]

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

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

6-Chloro-4-methoxypyridine-3-carbonitrile(1187190-69-7)1HNMR
6-Chloro-4-methoxypyridine-3-carbonitrile(1187190-69-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

4,6-DICHLORONICOTINONITRILE

166526-03-0

Sodium Methoxide

124-41-4

6-Chloro-4-methoxypyridine-3-carbonitrile

1187190-69-7

Synthesis of 6-chloro-4-methoxy-3-cyanopyridine (2): to a solution of 4,6-dichloronicotinonitrile (1) (200 mg, 1.06 mmol) in anhydrous methanol (10 mL) was added sodium methanol solution (0.5 M in MeOH, 2.12 mL, 1.06 mmol). The reaction mixture was stirred at 60 °C overnight. After completion of the reaction, the mixture was cooled to room temperature and neutralized by addition of hydrochloric acid (1 M, 8 mL). Subsequently, the volatile components were removed by distillation under reduced pressure. The product was purified by a Biotage fast chromatography system (elution gradient: 10%-50% ethyl acetate/hexane) to afford 6-chloro-4-methoxy-3-cyanopyridine (150 mg, 77% yield). The structure of the product was confirmed by 1H NMR (400 MHz, chloroform-d): δ 8.48 (s, 1H), 6.98 (s, 1H), 4.03 (s, 3H).

[References]

[1] Patent: US2015/291629, 2015, A1. Location in patent: Paragraph 1104
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