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

Thionyl Chloride → 3-(2-chloroethyl)-1-methyl-2,4(1H,3H)-quinazolinedione

HRID 477674
노트
인쇄 미리보기

반응식

HRID 477674 반응식
O[CH2:2][CH2:3][N:4]1[C:13](=[O:14])[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[N:6]([CH3:15])[C:5]1=[O:16].S(Cl)([Cl:19])=O>ClC(Cl)Cl>[Cl:19][CH2:2][CH2:3][N:4]1[C:13](=[O:14])[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[N:6]([CH3:15])[C:5]1=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 149898923-(2-hydroxyethyl)-1-methyl-2,4(1H,3H)-quinazolinedione

생성물 1

HCID 149898933-(2-chloroethyl)-1-methyl-2,4(1H,3H)-quinazolinedione수율 95%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A mixture of 4.5 parts of 3-(2-hydroxyethyl)-1-methyl-2,4(1H,3H)-quinazolinedione, 8 parts of thionyl chloride and 75 parts of trichloromethane was stirred and refluxed for 5 hours. The reaction mixture was evaporated, yielding 4.5 parts (95%) of 3-(2-chloroethyl)-1-methyl-2,4(1H,3H)-quinazolinedione as a residue (intermediate 171).

후처리

  1. temperaturerefluxed for 5 hours
  2. customThe reaction mixture was evaporated

출처 및 근거

ORD 기록
ord-2b68d0fbcd524debb438329d405ff965
출처 데이터셋
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04888426

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트