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Pyridine → 4-Nitro-N-(2-thiazolyl)benzamide

HRID 2243433
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HRID 2243433 반응식
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][N:6]=1.N1C=CC=CC=1.[N+:13]([C:16]1[CH:24]=[CH:23][C:19]([C:20](Cl)=[O:21])=[CH:18][CH:17]=1)([O-:15])=[O:14]>ClCCCl>[N+:13]([C:16]1[CH:17]=[CH:18][C:19]([C:20]([NH:1][C:2]2[S:3][CH:4]=[CH:5][N:6]=2)=[O:21])=[CH:23][CH:24]=1)([O-:15])=[O:14]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 21552-AminothiazoleHCID 85024-Nitrobenzoyl chloride

생성물 1

HCID 2303634-Nitro-N-(2-thiazolyl)benzamide수율 96%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매2회

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온도
60 °C

실험 절차

2-Aminothiazole (100 mmol) was suspended in 1,2-dichloroethane (200 mL) and pyridine (100 mmol) was added. The mixture was added portion wise to a suspension of 4-nitro benzoic acid chloride (150 mmol) in 1,2-dichloroethane (500 mL) and stirred at 60° C. over night. The reaction mixture was cooled and filtered. The filtrate was washed with 1,2-dichloroethane and dried in vacuo to give 4-nitro-N-thiazol-2-yl-benzamide.

후처리

  1. additionThe mixture was added portion
  2. temperatureThe reaction mixture was cooled
  3. filtrationfiltered
  4. washThe filtrate was washed with 1,2-dichloroethane
  5. customdried in vacuo

출처 및 근거

ORD 기록
ord-897392f68707407c831bba52d0a22bb6
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07674912B2

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