Trifluoroacetic acid → (R)-N-(3-amino-1-(3-fluoro-4-(trifluoromethyl)phenyl)propyl)-2-(isopropylamino)-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxamide
反応式
[F:1][C:2]1[CH:3]=[C:4]([C@H:12]([NH:23][C:24]([N:26]2[CH2:35][CH2:34][C:33]3[CH:32]=[N:31][C:30]([NH:36][CH:37]([CH3:39])[CH3:38])=[N:29][C:28]=3[CH2:27]2)=[O:25])[CH2:13][CH2:14][NH:15]C(=O)OC(C)(C)C)[CH:5]=[CH:6][C:7]=1[C:8]([F:11])([F:10])[F:9].C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH2:15][CH2:14][CH2:13][C@@H:12]([NH:23][C:24]([N:26]1[CH2:35][CH2:34][C:33]2[CH:32]=[N:31][C:30]([NH:36][CH:37]([CH3:39])[CH3:38])=[N:29][C:28]=2[CH2:27]1)=[O:25])[C:4]1[CH:5]=[CH:6][C:7]([C:8]([F:10])([F:9])[F:11])=[C:2]([F:1])[CH: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
To a solution 292 (0.090 g, 0.16 mmol) and DCM (3 mL) at RT was added TFA (1 mL) and the reaction was stirred at RT for 1 h and then concentrated to dryness. The resulting product was next dissolved in minimal DCM (using MeOH to aid solubility) and added to a stirring solution of 1M HCl in ether. The resulting solid was filtered, washed with ether and dried to afford 0.060 g (75%) of I-72: MS m/z (APCI-pos) M+1=455.
後処理
- concentrationconcentrated to dryness
- dissolutionThe resulting product was next dissolved in minimal DCM (using MeOH to aid solubility)
- additionadded to a stirring solution of 1M HCl in ether
- filtrationThe resulting solid was filtered
- washwashed with ether
- customdried
- customto afford 0.060 g (75%) of I-72
出典と根拠
- ORDレコード
- ord-fc6100b03d6545acaa70112e9f878331
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09133187B2
反応ノート
読み込み中…