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

4-Fluorobenzylic alcohol → 1-Benzyl-7-(4-fluorobenzyloxy)-2-methylpyrrolo[2,3-d]pyridazine

HRID 1734527
노트
인쇄 미리보기

반응식

HRID 1734527 반응식
CC(C)([O-])C.[K+].[F:7][C:8]1[CH:15]=[CH:14][C:11]([CH2:12][OH:13])=[CH:10][CH:9]=1.[CH2:16]([N:23]1[C:27]2=[C:28](Cl)[N:29]=[N:30][CH:31]=[C:26]2[CH:25]=[C:24]1[CH3:33])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>CN1CCCC1=O>[CH2:16]([N:23]1[C:27]2=[C:28]([O:13][CH2:12][C:11]3[CH:14]=[CH:15][C:8]([F:7])=[CH:9][CH:10]=3)[N:29]=[N:30][CH:31]=[C:26]2[CH:25]=[C:24]1[CH3:33])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 680224-Fluorobenzylic alcoholHCID 194377481-Benzyl-7-chloro-2-methylpyrrolo[2,3-d]pyridazineHCID 23665647Potassium tert-butoxide

생성물 1

HCID 194377621-Benzyl-7-(4-fluorobenzyloxy)-2-methylpyrrolo[2,3-d]pyridazine

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매2회

실험 절차

32.65 g (291 mmol) of potassium tert-butoxide and 1.54 g (5.82 mmol) of [18]crown-6 (98% strength) are added successively to a solution of 21.8 g (173 mmol) of 4-fluorobenzyl alcohol in 150 ml of anhydrous N-methylpyrrolidone. This mixture is stirred at room temperature for 1 h. A solution of 15.0 g (58.2 mmol) of 1-benzyl-7-chloro-2-methylpyrrolo[2,3-d]pyridazine in 100 ml of anhydrous N-methylpyrrolidone is subsequently added dropwise in the course of 30 min. The mixture is stirred at room temperature for a further 15 min, then treated with 500 ml of ice-water and extracted with 3×400 ml of ethyl acetate. The organic extracts are washed with 3×300 ml of water and subsequently dried over magnesium sulfate. After concentration and crystallization from diisopropyl ether, 12.95 g (64%) of the title compound are isolated. M.p.: 127°-132° C.

후처리

  1. stirringThe mixture is stirred at room temperature for a further 15 min
  2. extractionextracted with 3×400 ml of ethyl acetate
  3. washThe organic extracts are washed with 3×300 ml of water
  4. dry with materialsubsequently dried over magnesium sulfate
  5. concentrationAfter concentration and crystallization from diisopropyl ether, 12.95 g (64%) of the title compound
  6. customare isolated

출처 및 근거

ORD 기록
ord-a35c6760b2df472c893b8d9bcbe7e10e
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05534515

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트