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

Phenyl Isothiocyanate → 1-(4-Hydroxybutyl)-3-(3-phenylthioureido)pyrazole

HRID 544563
노트
인쇄 미리보기

반응식

HRID 544563 반응식
[NH2:1][C:2]1[CH:6]=[CH:5][N:4]([CH2:7][CH2:8][CH2:9][CH2:10][OH:11])[N:3]=1.[C:12]1([N:18]=[C:19]=[S:20])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C(#N)C>[OH:11][CH2:10][CH2:9][CH2:8][CH2:7][N:4]1[CH:5]=[CH:6][C:2]([NH:1][C:19]([NH:18][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[S:20])=[N:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7673Phenyl IsothiocyanateHCID 204512994-(3-amino-1H-pyrazol-1-yl)butan-1-ol

생성물 1

HCID 540150271-(4-Hydroxybutyl)-3-(3-phenylthioureido)pyrazole수율 29%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of 3-amino-1-(4-hydroxybutyl)pyrazole (1.0 g.) in dry acetonitrile (3 ml.) was slowly added phenylisothiocyanate (0.95 g.) and the mixture was stirred at room temperature for 17 hours. The solvent was evaporated and the residue purified by column chromatography on silica gel using EtOAc as eluant to give 1-(4-hydroxybutyl)-3-(3-phenylthioureido)pyrazole (0.54 g.; 29%), m.p. 112°-117°.

후처리

  1. customThe solvent was evaporated
  2. customthe residue purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-bb1c2e5ff6a449c18db79a5c178c6732
출처 데이터셋
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04451463

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트