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2-Aminothiophenol → N-benzyloxycarbonyl-S-(2-aminophenyl)cysteine

HRID 1719101
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인쇄 미리보기

반응식

HRID 1719101 반응식
[CH2:1]([O:8][C:9]([NH:11][C:12](=[CH2:16])[C:13]([OH:15])=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[SH:24]>C(O)C>[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:13]([OH:15])=[O:14])[CH2:16][S:24][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=1[NH2:17])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 87132-AminothiophenolHCID 4674477Z-dehydro-Ala-OH

생성물 1

HCID 57289832N-benzyloxycarbonyl-S-(2-aminophenyl)cysteine수율 49.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

23 g of α-benzyloxycarbonylaminoacrylic acid and 30 g of 2-aminobenzenethiol were dissolved in 20 ml of ethanol, and the resulting mixture was stirred at room temperature for an hour. After the solvent was distilled off, ether was added to the residue so as to cause crystallization. The precipitated crystals were separated by filtration and washed with ether to obtain 17.8 g of the desired compound. Its melting point was 150°-151° C.

후처리

  1. distillationAfter the solvent was distilled off
  2. additionether was added to the residue so as
  3. customcrystallization
  4. customThe precipitated crystals were separated by filtration
  5. washwashed with ether

출처 및 근거

ORD 기록
ord-c8d3c246ed8b402ebc4fc361dd0d0feb
출처 데이터셋
uspto-grants-1985_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04539151

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