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Ammonia → 2-Amino-4,6-dimethyl-5-phenylpyridine-3-carbonitrile

HRID 1980316
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반응식

HRID 1980316 반응식
Cl[C:2]1[C:7]([C:8]#[N:9])=[C:6]([CH3:10])[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:4]([CH3:17])[N:3]=1.[NH3:18]>CS(C)=O>[NH2:18][C:2]1[C:7]([C:8]#[N:9])=[C:6]([CH3:10])[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:4]([CH3:17])[N:3]=1
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참가 물질

4

반응물 2

HCID 222Ammonia2회HCID 135028532-Chloro-4,6-dimethyl-5-phenylpyridine-3-carbonitrile

생성물 1

HCID 204025382-Amino-4,6-dimethyl-5-phenylpyridine-3-carbonitrile

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

2-Chloro-4,6-dimethyl-5-phenyl-3-pyridinecarbonitrile (8.3 grams) was dissolved in 110 ml DMSO and treated with gaseous NH3 at a temperature of 100°-110° C. After about 66 hours of heating and treatment with NH3, the reaction mixture was cooled and poured into ice water. A solid precipitate formed which was collected, washed with water, and then dried in an oven desicator. The identity of the desired product was confirmed by NMR.

후처리

  1. temperatureAfter about 66 hours of heating
  2. customA solid precipitate formed which
  3. customwas collected
  4. washwashed with water
  5. customdried in an oven desicator

출처 및 근거

ORD 기록
ord-4e8689eb7dbe45b1b3678dccde416c11
출처 데이터셋
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04508722

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