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

Benzenecarboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide → 3-benzenesulfonylmethyl-5-phenyl-1H-[1,2,4]triazole

HRID 277032
노트
인쇄 미리보기

반응식

HRID 277032 반응식
[NH2:1][C:2](=[N:13][NH:14][C:15]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=O)[CH2:3][S:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=[O:6])=[O:5]>C(O)C>[C:7]1([S:4]([CH2:3][C:2]2[N:1]=[C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[NH:14][N:13]=2)(=[O:6])=[O:5])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86757848Benzenecarboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide

생성물 1

HCID 1785273983-benzenesulfonylmethyl-5-phenyl-1H-[1,2,4]triazole수율 75.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

93.1 g (0.29 mol) Benzenecarboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide were heated at 200° C. for 30 minutes. The molten mass was then cooled, dissolved in 500 ml hot ethanol and stirred for 15 hous at room temperature. The precipitated crystals were filtered off and dried to yield 65.6 g (75%) 3-benzenesulfonylmethyl-5-phenyl-1H-[1,2,4]triazole with mp. 141-144° C. MS m/e (%): 299 (M+, 100).

후처리

  1. temperature
The molten mass was then cooled
  • filtrationThe precipitated crystals were filtered off
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-75df46af844c4cd7b370a4fa3cefcd29
    출처 데이터셋
    uspto-grants-2002_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06355653B1

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트