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

1-benzyl-3-(3-chloropropyl)-5-methyl-2,4(1H,3H)-pyrimidinedione → 3-(3-chloropropyl)-5-methyl-2,4(1H,3H)-pyrimidinedione

HRID 342555
노트
인쇄 미리보기

반응식

HRID 342555 반응식
C([N:8]1[CH:13]=[C:12]([CH3:14])[C:11](=[O:15])[N:10]([CH2:16][CH2:17][CH2:18][Cl:19])[C:9]1=[O:20])C1C=CC=CC=1>[Pd].C([O-])=O.[NH4+].CO>[Cl:19][CH2:18][CH2:17][CH2:16][N:10]1[C:11](=[O:15])[C:12]([CH3:14])=[CH:13][NH:8][C:9]1=[O:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 111199111-benzyl-3-(3-chloropropyl)-5-methyl-2,4(1H,3H)-pyrimidinedione

생성물 1

HCID 110418353-(3-chloropropyl)-5-methyl-2,4(1H,3H)-pyrimidinedione수율 75.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 86753564Ammonium formate methanol용매

반응 조건

온도
25 °C

실험 절차

A mixture of 1-benzyl-3-(3-chloropropyl)-5-methyl-2,4(1H,3H)-pyrimidinedione (1 g, 3.41 mmol), prepared as in Example 19, 10% palladium on carbon (1 g) and 0.1M ammonium formate/methanol (340 mL) was heated 3 hours at reflux under argon. The reaction mixture was allowed to cool to 25° C., then filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane-ethyl acetate (1:1) to give 3-(3-chloropropyl)-5-methyl-2,4(1H,3H)-pyrimidinedione (0.52 g, 2.57 mmol), m.p. 117°-121° C.

후처리

  1. temperaturewas heated 3 hours
  2. temperatureat reflux under argon
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography on silica gel eluting with hexane-ethyl acetate (1:1)

출처 및 근거

ORD 기록
ord-97df699b140b4ed1bcd97f5f7a02ca66
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05859014

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트