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2-Imidazolidinethione, 4,4-dimethyl- → HCID 22760449, 화합물

HRID 461138
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HRID 461138 반응식
[Br:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([Cl:11])=[C:7]([S:12](=[O:15])(=[O:14])[NH2:13])[CH:6]=1)=[O:4].[CH3:16][C:17]1([CH3:23])[CH2:21][NH:20][C:19](=[S:22])[NH:18]1>CO>[BrH:1].[Cl:11][C:8]1[CH:9]=[CH:10][C:5]([C:3]2([OH:4])[CH2:2][S:22][C:19]3=[N:18][C:17]([CH3:23])([CH3:16])[CH2:21][N:20]23)=[CH:6][C:7]=1[S:12](=[O:15])(=[O:14])[NH2:13]
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참가 물질

4

반응물 2

HCID 30325022-Imidazolidinethione, 4,4-dimethyl-HCID 12952390Bromo-4'-chloro-3'-sulfamoylacetophenone

생성물 1

HCID 22760449HCID 22760449, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

3.1 g of 2-bromo-4'-chloro-3'-sulfamoylacetophenone and 1.3 g of 4,4-dimethyl-2-imidazolidine-thione were reacted as described in Example 12 in 15 ml of methanol, the reaction mixture was precipitated with 70 ml of diethyl ether and the oily precipitate was crystallized with ethyl acetate at 40° to 50° C. Colorless, crystalline solid body: melting point: 164° C (decomposition).

후처리

  1. customthe reaction mixture was precipitated with 70 ml of diethyl ether
  2. customthe oily precipitate was crystallized with ethyl acetate at 40° to 50° C

출처 및 근거

ORD 기록
ord-6d567a643e8b45d3977e2d9564a01522
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04061761

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