반응식
[CH3:1][N:2]1[C:6]([CH3:7])=[N:5][N:4]=[N:3]1.C([Li])CCC.[F:13][C:14]1[CH:29]=[C:28]([CH3:30])[CH:27]=[CH:26][C:15]=1[C:16]([C:18]1[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][C:19]=1[F:25])=[O:17]>O1CCCC1>[F:13][C:14]1[CH:29]=[C:28]([CH3:30])[CH:27]=[CH:26][C:15]=1[C:16]([C:18]1[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][C:19]=1[F:25])([OH:17])[CH2:7][C:6]1[N:2]([CH3:1])[N:3]=[N:4][N:5]=1참가 물질
반응 조건
- 온도
- -10 °C
실험 절차
To a solution of 1,5-dimethyltetrazole (4.6 g, 4.7 mmoles) in tetrahydrofuran (40 mL) at -50° C. was added butyl lithium solution (21.4 mL of a 2.2 M solution, 4.7 mmoles). After stirring for 10 minutes, a solution of 2,2'-difluoro-4,4'-dimethylbenzophenone in tetrahydrofuran (15 mL) was added. The solution was stirred for 2.5 hours during which time it was allowed to warm to -10° C. The reaction was quenched by adding 1N hydrochloric acid. The layers were separated and the aqueous layer was extracted with methylene chloride. The combined organic fractions were dried (MgSO4) was evaporated. The residue was triturated with diethyl ether and crystallized from isopropyl acetate to give 8.0 g of the title compound; m.p.=150°-151° C. MS: M+ =344.
후처리
- stirringThe solution was stirred for 2.5 hours during which time it
- customThe reaction was quenched
- additionby adding 1N hydrochloric acid
- customThe layers were separated
- extractionthe aqueous layer was extracted with methylene chloride
- dry with materialThe combined organic fractions were dried (MgSO4)
- customwas evaporated
- customThe residue was triturated with diethyl ether
- customcrystallized from isopropyl acetate
출처 및 근거
- ORD 기록
- ord-0ba3bcc335f14299b184f675ef605af0
- 출처 데이터셋
- uspto-grants-1991_11
- 특허 번호
- US05068346
연결된 노트
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