홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

ethyl N-(4-p-nitrophenyl-2-thiazolyl)carbamate → ethyl N-(4-p-aminophenyl-2-thiazolyl)carbamate

HRID 1980825
노트
인쇄 미리보기

반응식

HRID 1980825 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:11]=[C:12]([NH:15][C:16](=[O:20])[O:17][CH2:18][CH3:19])[S:13][CH:14]=2)=[CH:6][CH:5]=1)([O-])=O.[H][H]>C(OCC)(=O)C.[Pd]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:11]=[C:12]([NH:15][C:16](=[O:20])[O:17][CH2:18][CH3:19])[S:13][CH:14]=2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 5108134ethyl N-(4-p-nitrophenyl-2-thiazolyl)carbamateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 15916633ethyl N-(4-p-aminophenyl-2-thiazolyl)carbamate수율 72.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

In 500 ml of ethyl acetate, was dissolved 4 g of ethyl N-(4-p-nitrophenyl-2-thiazolyl)carbamate, followed by an addition of 3 g of a 10% palladium/carbon catalyst. The mixture was then subjected under normal pressure to reduction with hydrogen gas. The catalyst was filtered off. The filtrate was concentrated and subjected to column chromatography on silica gel. The reaction product was eluted with a chloroform/ethylacetate mixed solvent. The resulting product was then recrystallized from methanol to obtain 2.6 g of ethyl N-(4-p-aminophenyl-2-thiazolyl)carbamate.

후처리

  1. filtrationThe catalyst was filtered off
  2. concentrationThe filtrate was concentrated
  3. washThe reaction product was eluted with a chloroform/ethylacetate mixed solvent
  4. customThe resulting product was then recrystallized from methanol

출처 및 근거

ORD 기록
ord-a8636db37ef64995bc39fcef3690ec6f
출처 데이터셋
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04511574

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트