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2-(4-Chlorophenyl)-4-methyl-1,3-thiazole-5-carbohydrazide → HCID 68642106, 화합물

HRID 1498951
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HRID 1498951 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:9][C:10]([C:14]([NH:16][NH2:17])=[O:15])=[C:11]([CH3:13])[N:12]=2)=[CH:4][CH:3]=1.[OH:18][C:19]1[CH:20]=[C:21]([CH:25]=[CH:26][C:27]=1[O:28][CH3:29])[C:22](Cl)=[O:23]>N1C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:9][C:10]([C:14]([NH:16][NH:17][C:22](=[O:23])[C:21]3[CH:25]=[CH:26][C:27]([O:28][CH3:29])=[C:19]([OH:18])[CH:20]=3)=[O:15])=[C:11]([CH3:13])[N:12]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 27435212-(4-Chlorophenyl)-4-methyl-1,3-thiazole-5-carbohydrazideHCID 450815953-Hydroxy-4-methoxybenzoyl chloride

생성물 1

HCID 68642106HCID 68642106, 화합물수율 24.6%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

In pyridine (4 ml), 2-(4-chloro-phenyl)-4-methyl-thiazole-5-carboxylic acid hydrazide (120 mg) and 3-hydroxy-4-methoxy-benzoyl chloride (84 mg) were stirred for 24 hours at a room temperature. The mixture was concentrated under a reduced pressure, and then diluted hydrochloric acid was added thereto. The precipitated crystal was separated by filtration and dried, and the resulting crystal was recrystallized from ethanol to give the title compound (46 mg, 24%).

후처리

  1. concentrationThe mixture was concentrated under a reduced pressure
  2. additiondiluted hydrochloric acid was added
  3. customThe precipitated crystal was separated by filtration
  4. customdried
  5. customthe resulting crystal was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-d17013868eb3410485917c3732d660ea
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09200008B2

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