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Chloride → 2-(4-Chlorobenzoylamino)-4,5-dimethoxybenzamide

HRID 1166149
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HRID 1166149 반응식
[NH2:1][C:2]1[CH:10]=[C:9]([O:11][CH3:12])[C:8]([O:13][CH3:14])=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].[Cl:15][C:16]1[CH:24]=[CH:23][C:19]([C:20](Cl)=[O:21])=[CH:18][CH:17]=1.[Cl-]>C(N(CC)CC)C>[Cl:15][C:16]1[CH:24]=[CH:23][C:19]([C:20]([NH:1][C:2]2[CH:10]=[C:9]([O:11][CH3:12])[C:8]([O:13][CH3:14])=[CH:7][C:3]=2[C:4]([NH2:6])=[O:5])=[O:21])=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 312ChlorideHCID 85014-Chlorobenzoyl chlorideHCID 108672362-Amino-4,5-dimethoxybenzamide

생성물 1

HCID 229974052-(4-Chlorobenzoylamino)-4,5-dimethoxybenzamide

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

A mixture of 13.7 g of 2-amino-4,5-dimethoxybenzamide, 8.1 g of triethylamine, 13.8 g of 4-chlorobenzoyl chloride and 300 ml of methylene. chloride was stirred for 2 h without cooling. The precipitate was filtered off with suction, stirred with water, filtered off with suction and dried under reduced pressure. Yield: 22.5 g. M.p.: 243° C.

후처리

  1. temperaturewithout cooling
  2. filtrationThe precipitate was filtered off with suction
  3. filtrationfiltered off with suction
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-613e2bffac8c4b2e949d650e7fa53372
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06613772B1

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