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

4-(6-fluoropyridin-3-yl)-1H-pyrrol-2(5H)-one → 4-(6-Fluoropyridin-3-yl)pyrrolidin-2-one

HRID 595922
노트
인쇄 미리보기

반응식

HRID 595922 반응식
[F:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH2:12][NH:11][C:10](=[O:13])[CH:9]=2)=[CH:4][CH:3]=1>CO.[Pd]>[F:1][C:2]1[N:7]=[CH:6][C:5]([CH:8]2[CH2:12][NH:11][C:10](=[O:13])[CH2:9]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 1180452444-(6-fluoropyridin-3-yl)-1H-pyrrol-2(5H)-one

생성물 1

HCID 1180464264-(6-Fluoropyridin-3-yl)pyrrolidin-2-one수율 80%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To 4-(6-fluoropyridin-3-yl)-1H-pyrrol-2(5H)-one(190 mg, 1.066 mmol) in MeOH (10 mL) under N2 atmosphere was added Pd—C (227 mg, 0.213 mmol). The reaction mixture was stirred under H2 balloon at room temperature for overnight. Reaction mixture was filtered through Celite, washed with MeOH. Filtrate was evaporated. Azeotrope with toluene (x=3). Yield was 80%. Proceed for next step. LCMS (m/z): 181.0 (MH+), 0.341 min.

후처리

  1. customReaction mixture
  2. filtrationwas filtered through Celite
  3. washwashed with MeOH
  4. customFiltrate was evaporated
  5. custom181.0 (MH+), 0.341 min.

출처 및 근거

ORD 기록
ord-9229717d83af421c9cbec786ffe28491
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242996B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트