Boron tribromide → (S)-1-(3-(4-Amino-6-((1-(5-methyl-4-oxo-3-phenyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl)amino)pyrimidin-5-yl)-5-hydroxyphenyl)urea
反応式
[NH2:1][C:2]1[C:7]([C:8]2[CH:9]=[C:10]([NH:16][C:17]([NH2:19])=[O:18])[CH:11]=[C:12]([O:14]C)[CH:13]=2)=[C:6]([NH:20][C@H:21]([C:23]2[N:28]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[C:27](=[O:35])[C:26]3=[C:36]([CH3:39])[CH:37]=[CH:38][N:25]3[N:24]=2)[CH3:22])[N:5]=[CH:4][N:3]=1.B(Br)(Br)Br>ClCCl>[NH2:1][C:2]1[C:7]([C:8]2[CH:9]=[C:10]([NH:16][C:17]([NH2:19])=[O:18])[CH:11]=[C:12]([OH:14])[CH:13]=2)=[C:6]([NH:20][C@H:21]([C:23]2[N:28]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[C:27](=[O:35])[C:26]3=[C:36]([CH3:39])[CH:37]=[CH:38][N:25]3[N:24]=2)[CH3:22])[N:5]=[CH:4][N:3]=1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
(S)-1-(3-(4-Amino-6-((1-(5-methyl-4-oxo-3-phenyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl)amino)pyrimidin-5-yl)-5-methoxyphenyl)urea (50 mg, 0.10 mmol) was dissolved in dichloromethane (1.5 ml). A solution of boron tribromide (1M in dichloromethane, 285 μl, 0.29 mmol) was added dropwise and the reaction was stirred at room temperature overnight. The mixture was diluted with dichloromethane and washed with a solution of 4% sodium bicarbonate, water, brine and dried over sodium sulphate, filtered and evaporated under reduced pressure. The product was purified by reverse phase using SP1® Purification System to give 27 mg (55% yield) of the title compound. Purity 100%.
後処理
- washwashed with a solution of 4% sodium bicarbonate, water, brine
- dry with materialdried over sodium sulphate
- filtrationfiltered
- customevaporated under reduced pressure
- customThe product was purified by reverse phase
- custom® Purification System
出典と根拠
- ORDレコード
- ord-f166c93910f743f283d0f7a4f014782a
- 出典データセット
- uspto-grants-2016_07
- 特許番号
- US09388189B2
反応ノート
読み込み中…