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

m-Chloroperbenzoic acid → Acetic acid 1-ethylcarbamoyl-7-oxiranylmethyl-1H-indazol-6-yl ester

HRID 2121859
노트
인쇄 미리보기

반응식

HRID 2121859 반응식
[CH2:1]([C:4]1[C:5]([O:18][C:19](=[O:21])[CH3:20])=[CH:6][CH:7]=[C:8]2[C:12]=1[N:11]([C:13](=[O:17])[NH:14][CH2:15][CH3:16])[N:10]=[CH:9]2)[CH:2]=[CH2:3].ClC1C=CC=C(C(OO)=[O:30])C=1>ClCCl>[CH2:15]([NH:14][C:13]([N:11]1[C:12]2[C:8](=[CH:7][CH:6]=[C:5]([O:18][C:19](=[O:21])[CH3:20])[C:4]=2[CH2:1][CH:2]2[CH2:3][O:30]2)[CH:9]=[N:10]1)=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 69564705Acetic Acid 7-allyl-1-ethylcarbamoyl-1H-indazol-6-yl ester

생성물 1

HCID 86759647Acetic acid 1-ethylcarbamoyl-7-oxiranylmethyl-1H-indazol-6-yl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of the product from Step D (2.70 g, 9.4 mmol) in dichloromethane (15 mL) was added 3-chloro-perbenzoic acid (2.31 g, 10.3 mmol, 77% pure) and the mixture stirred at ambient temperature for 1 h. Additional 3-chloro-perbenzoic (0.2 g, 0.9 mmol) was added and the reaction continued for 3 h. The reaction was quenched with saturated aqueous sodium bicarbonate (100 mL) and extracted with dichloromethane (50 mL). The extract was dried (MgSO4) and evaporated to a white solid (1.59 g, 56%): mp 110-111° C.; LC/MS (+APCI) m/z 304 (M+H).

후처리

  1. additionAdditional 3-chloro-perbenzoic (0.2 g, 0.9 mmol) was added
  2. waitthe reaction continued for 3 h
  3. customThe reaction was quenched with saturated aqueous sodium bicarbonate (100 mL)
  4. extractionextracted with dichloromethane (50 mL)
  5. dry with materialThe extract was dried (MgSO4)
  6. customevaporated to a white solid (1.59 g, 56%)

출처 및 근거

ORD 기록
ord-e68768dbd2c54608991dacfeb68f3fd0
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06696476B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트