Trifluoroacetic acid water → Trifluoroacetic acid
反応式
C[Si](C)(C)CCOC[N:7](COCC[Si](C)(C)C)[C:8]1[N:13]2[N:14]=[CH:15][C:16]([C:17]3[CH:18]=[N:19][C:20]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)=[CH:21][CH:22]=3)=[C:12]2[N:11]=[C:10]([CH:29]2[CH2:34][CH2:33][N:32](C(OC(C)(C)C)=O)[CH2:31][CH2:30]2)[C:9]=1[C:42]#[N:43].[C:54]([OH:60])([C:56]([F:59])([F:58])[F:57])=[O:55].O>>[NH2:7][C:8]1[N:13]2[N:14]=[CH:15][C:16]([C:17]3[CH:18]=[N:19][C:20]([C:23]4[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=4)=[CH:21][CH:22]=3)=[C:12]2[N:11]=[C:10]([CH:29]2[CH2:30][CH2:31][NH:32][CH2:33][CH2:34]2)[C:9]=1[C:42]#[N:43].[C:54]([OH:60])([C:56]([F:59])([F:58])[F:57])=[O:55]参加物
4
反応物 2
生成物 2
実験手順
Tert-butyl 4-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)-6-cyano-3-(6-phenylpyridin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)piperidine-1-carboxylate (190 mg) was treated with TFA/water (95:5, 3 ml) with stirring for 10 minutes. The reaction mixture was concentrated and lyophilized to yield the title compound as TFA salt.
後処理
- concentrationThe reaction mixture was concentrated
出典と根拠
- ORDレコード
- ord-a017eaafbadd4a2f99d2ac8bb36f594e
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08591943B2
反応ノート
読み込み中…