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Hydrochloric Acid → HCID 21430443, 화합물

HRID 437168
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인쇄 미리보기

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HRID 437168 반응식
[CH2:1]([NH:4][S:5]([C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][C:16]=1[Cl:17])[C:11]([OH:13])=[O:12])(=[O:7])=[O:6])[CH:2]=[CH2:3].[CH3:18][N:19]1[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]1.Cl>CN(C)C=O>[ClH:17].[CH2:1]([NH:4][S:5]([C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][C:16]=1[N:22]1[CH2:23][CH2:24][N:19]([CH3:18])[CH2:20][CH2:21]1)[C:11]([OH:13])=[O:12])(=[O:7])=[O:6])[CH:2]=[CH2:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 531671-MethylpiperazineHCID 25559564-Chloro-3-[(prop-2-en-1-yl)sulfamoyl]benzoic acid

생성물 1

HCID 21430443HCID 21430443, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
140 °C

실험 절차

A mixture of 28 g of 3-allylsulfamoyl-4-chlorobenzoic acid, 30 g of N-methylpiperazine and 20 ml of dimethylformamide was heated for 4 hours at 140° C. When the reaction solution was subsequently introduced into 0.3 l of 2N HCl, the monohydrochloride crystallized immediately. The product was then purified by recrystallization from water.

후처리

  1. customthe monohydrochloride crystallized immediately
  2. customThe product was then purified by recrystallization from water

출처 및 근거

ORD 기록
ord-22db37c1153c4e6eb2315d84f5487608
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04029787

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