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

Toluene → N-{4-[(1,2-Benzothiazol-5-yl)oxy]phenyl}-N'-methylurea

HRID 280433
노트
인쇄 미리보기

반응식

HRID 280433 반응식
[NH2:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:8]=[CH:9][C:10]3[S:14][N:13]=[CH:12][C:11]=3[CH:15]=2)=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.[CH3:25][N:26]=[C:27]=[O:28]>C(N(CC)CC)C>[CH3:25][NH:26][C:27]([NH:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:8]=[CH:9][C:10]3[S:14][N:13]=[CH:12][C:11]=3[CH:15]=2)=[CH:4][CH:3]=1)=[O:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1140TolueneHCID 12228Methyl IsocyanateHCID 132693984-[(1,2-Benzothiazol-5-yl)oxy]aniline

생성물 1

HCID 13269403N-{4-[(1,2-Benzothiazol-5-yl)oxy]phenyl}-N'-methylurea수율 85%

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

24.2 parts of 5-(4'-aminophenoxy)-benzisothiazole, 400 parts of toluene, 1 part of triethylamine and 11.4 parts of methyl isocyanate were heated at 80° C. for 12 hours, and the reaction mixture was then evaporated down under reduced pressure. 25 parts (85% of theory) of 5-(4'-methylaminocarbonylaminophenoxy)-benzisothiazole of melting point 178° C. were obtained.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customthe reaction mixture was then evaporated down under reduced pressure

출처 및 근거

ORD 기록
ord-5fe0223b8e87453fb76a6d3ed74252cd
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04589910

반응 노트

불러오는 중…