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

Bromomethyl 4-methoxyphenyl ketone → HCID 23371609, 화합물

HRID 1757391
노트
인쇄 미리보기

반응식

HRID 1757391 반응식
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[CH2:8][CH2:9][C:10](=[O:13])[NH:11][N:12]=2)=[CH:3][CH:2]=1.[CH3:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]([CH2:24][Br:25])=[O:23])=[CH:18][CH:17]=1>C(O)C>[Br-:25].[CH3:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]([CH2:24][N+:1]2[CH:6]=[CH:5][C:4]([C:7]3[CH2:8][CH2:9][C:10](=[O:13])[NH:11][N:12]=3)=[CH:3][CH:2]=2)=[O:23])=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4965Bromomethyl 4-methoxyphenyl ketoneHCID 127640636-(Pyridin-4-yl)-4,5-dihydropyridazin-3(2H)-one

생성물 1

HCID 23371609HCID 23371609, 화합물수율 87%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4,5-Dihydro-6-(4-pyridyl)-pyridazin-3(2H)-one (175 mg, 1 mmol) and 4'-methoxyphenacyl bromide (252 mg, 1.1 mmol) were dissolved in absolute ethanol (5 ml), refluxed for two hours and then stirred at room temperature overnight. The resulting precipitate was collected by filtration and washed with absolute ethanol to obtain the titled compound (350 mg) as brown columns.

후처리

  1. temperaturerefluxed for two hours
  2. filtrationThe resulting precipitate was collected by filtration
  3. washwashed with absolute ethanol

출처 및 근거

ORD 기록
ord-f4805730aa814a2f90de20c0f551532d
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05446042

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트