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

Acetylthiourea → N-(4-[3-(2-hydroxyethyl)phenyl]-1,3-thiazol-2-yl}acetamide

HRID 1246547
노트
인쇄 미리보기

반응식

HRID 1246547 반응식
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH2:11][CH2:12][OH:13])[CH:6]=1)=O.[C:14]([NH:17][C:18]([NH2:20])=[S:19])(=[O:16])[CH3:15]>O1CCCC1>[OH:13][CH2:12][CH2:11][C:7]1[CH:6]=[C:5]([C:3]2[N:20]=[C:18]([NH:17][C:14](=[O:16])[CH3:15])[S:19][CH:2]=2)[CH:10]=[CH:9][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723593AcetylthioureaHCID 219151842-Bromo-1-[3-(2-hydroxyethyl)phenyl]ethanone

생성물 1

HCID 21915066N-(4-[3-(2-hydroxyethyl)phenyl]-1,3-thiazol-2-yl}acetamide수율 72.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

To a solution of 2-bromo-1-[3-(2-hydroxyethyl)phenyl]ethanone (crude, 658 mg) in tetrahydrofuran (15 ml) was added 1-acetyl-2-thiourea (320 mg) at 25° C. The mixture was stirred at 60° C. for 2 h. The residual colorless crystals were collected by filtration. The crystals were washed with isopropyl ether, dried under reduced pressure to give N-{4-[3-(2-hydroxyethyl)phenyl]-1,3-thiazol-2-yl}acetamide (514 mg) as a colorless crystal.

후처리

  1. filtrationThe residual colorless crystals were collected by filtration
  2. washThe crystals were washed with isopropyl ether
  3. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-ef312075cf6941d3a9d8f7a0ab070f1e
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07125901B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트