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

6-(6-Bromo-2,3,4-trifluorophenyl)-3,3-dimethylpiperidin-2-one → 3,3-Dimethyl-6-(2,3,4-trifluorophenyl)piperidin-2-one

HRID 1864851
노트
인쇄 미리보기

반응식

HRID 1864851 반응식
Br[C:2]1[C:7]([CH:8]2[NH:13][C:12](=[O:14])[C:11]([CH3:16])([CH3:15])[CH2:10][CH2:9]2)=[C:6]([F:17])[C:5]([F:18])=[C:4]([F:19])[CH:3]=1>[Pd].CCO>[CH3:15][C:11]1([CH3:16])[CH2:10][CH2:9][CH:8]([C:7]2[CH:2]=[CH:3][C:4]([F:19])=[C:5]([F:18])[C:6]=2[F:17])[NH:13][C:12]1=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 866163926-(6-Bromo-2,3,4-trifluorophenyl)-3,3-dimethylpiperidin-2-one2회

생성물 1

HCID 669732823,3-Dimethyl-6-(2,3,4-trifluorophenyl)piperidin-2-one

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution of 6-(6-bromo-2,3,4-trifluorophenyl)-3,3-dimethylpiperidin-2-one (27.0 mg, 0.080 mmol, described in Intermediate 17) and 10% palladium on carbon in degassed EtOH (2 mL) was stirred under a hydrogen balloon for 3 h. The reaction mixture was filtered through a Celite pad and concentrated in vacuo to provide the title compound. MS: m/z=258 (M+1).

후처리

  1. filtrationThe reaction mixture was filtered through a Celite pad
  2. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-aa802142768d48f1aa1d871cf556ed06
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07625901B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트