反応式
[N:1]1([CH2:6][C:7]([N:9]2[CH2:13][C@H:12]([C:14]#[N:15])[CH2:11][C@H:10]2[C:16]([NH:18][C:19]2[CH:24]=[CH:23][C:22]([O:25][C:26]3[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=3)=[CH:21][CH:20]=2)=[O:17])=[O:8])[CH:5]=[N:4][CH:3]=[N:2]1.[ClH:33]>[Pd].CO>[ClH:33].[N:1]1([CH2:6][C:7]([N:9]2[CH2:13][C@H:12]([CH2:14][NH2:15])[CH2:11][C@H:10]2[C:16]([NH:18][C:19]2[CH:24]=[CH:23][C:22]([O:25][C:26]3[CH:27]=[CH:28][C:29]([F:32])=[CH:30][CH:31]=3)=[CH:21][CH:20]=2)=[O:17])=[O:8])[CH:5]=[N:4][CH:3]=[N:2]1参加物
5
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
A flask was charged with (2S,4R)-1-(2-(1H-1,2,4-triazol-1-yl)acetyl)-4-cyano-N-(4-(4-fluorophenoxy)phenyl)pyrrolidine-2-carboxamide (260 mg, 0.599 mmol), prepared as in Reference 11, methanol (4 mL), hydrogen chloride (4N in dioxane, 16 mmol) and palladium on carbon (10%, 100 mg) and the mixture was placed under a hydrogen atmosphere (balloon). The mixture was stirred for 18 hours at ambient temperature, filtered and concentrated to give crude (2S,4S)-1-(2-(1H-1,2,4-triazol-1-yl)acetyl)-4-aminomethyl-N-(4-(4-fluorophenoxy)phenyl)pyrrolidine-2-carboxamide hydrochloride salt (0.247 g, 0.564 mmol).
後処理
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-e72b53e2622e451e906ea0a278078dac
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08791102B2
関連ノート
読み込み中…