Trichloroacetyl chloride → 2,2,2-Trichloro-1-{10-[(2-methoxy-2'-methyl-1,1'-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanone
反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([C:9]([N:11]2[C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=3[CH2:15][N:14]3[CH:22]=[CH:23][CH:24]=[C:13]3[CH2:12]2)=[O:10])[CH:6]=[CH:5][C:4]=1[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[CH3:31].C(N(CC)CC)C.[Cl:39][C:40]([Cl:45])([Cl:44])[C:41](Cl)=[O:42].C(OCC)(=O)C>ClCCl.C(Cl)(Cl)Cl>[Cl:39][C:40]([Cl:45])([Cl:44])[C:41]([C:22]1[N:14]2[C:13]([CH2:12][N:11]([C:9]([C:7]3[CH:6]=[CH:5][C:4]([C:25]4[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=4[CH3:31])=[C:3]([O:2][CH3:1])[CH:8]=3)=[O:10])[C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=3[CH2:15]2)=[CH:24][CH:23]=1)=[O:42]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 10-[(2-methoxy-2′-methyl-1,1′-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine of Step E (21 mmol) and triethylamine (43 mmol) in anhydrous dichloromethane (45 mL) was cooled in an ice bath. To the stirred solution was added, dropwise, trichloroacetyl chloride (65 mmol). The mixture was allowed to stir at ambient temperature for 72 hours, then was washed with 0.1 N hydrochloric acid and brine, and dried over anhydrous sodium sulfate. Evaporation yielded a foam that solidified by heating with ethyl acetate and chloroform to provide 10.2 g (85%) of the title compound as a white solid, m.p. 221-222° C. MS [(+)ESI, m/z]: 553 [M+H]+
後処理
- additionTo the stirred solution was added
- washwas washed with 0.1 N hydrochloric acid and brine
- dry with materialdried over anhydrous sodium sulfate
- customEvaporation
- customyielded a foam that solidified
出典と根拠
- ORDレコード
- ord-f0d1bddc9dba46c7981cc08e749090af
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07691848B2
反応ノート
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