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m-Chloroperbenzoic acid → 2-Amino-4-(4-aminophenylsulfinylmethyl)thiazole

HRID 2380590
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HRID 2380590 반응식
ClC1C=CC=C(C(OO)=[O:9])C=1.[NH2:12][C:13]1[S:14][CH:15]=[C:16]([CH2:18][S:19][C:20]2[CH:25]=[CH:24][C:23]([NH2:26])=[CH:22][CH:21]=2)[N:17]=1>ClCCl.CN(C)C=O>[NH2:12][C:13]1[S:14][CH:15]=[C:16]([CH2:18][S:19]([C:20]2[CH:25]=[CH:24][C:23]([NH2:26])=[CH:22][CH:21]=2)=[O:9])[N:17]=1
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참가 물질

5

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 15729148HCID 15729148, 화합물

생성물 1

HCID 189547392-Amino-4-(4-aminophenylsulfinylmethyl)thiazole수율 86.3%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 6344Dichloromethane용매2회

실험 절차

A solution of 3-chloroperbenzoic acid (4.9 g) in dichloromethane (100 ml) was dropwise added to a solution of 2-amino-4-(4-aminophenylthiomethyl)thiazole (5.1 g) in a mixture of dichloromethane (200 ml) and N,N-dimethylformamide (10 ml) at 5° C. with stirring. The mixture was stirred at 5° C. for 1.5 hours with stirring. The precipitates were collected by filtration, washed with ethyl acetate and dried in vacuo to give solid. The solid was recrystallized from ethanol to give 2-amino-4- (4-aminophenylsulfinylmethyl)thiazole (4.70 g, yield: 86.3%).

후처리

  1. stirringThe mixture was stirred at 5° C. for 1.5 hours
  2. stirringwith stirring
  3. filtrationThe precipitates were collected by filtration
  4. washwashed with ethyl acetate
  5. customdried in vacuo
  6. customto give solid
  7. customThe solid was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-229d8e0b7ddc45868dafe8a15fba33c0
출처 데이터셋
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05369107

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