2-(carbamoylamino)-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]acetamide → HCID 44595798、化合物
反応式
[C:1]([NH:4][CH2:5][C:6]([NH:8][C@@H:9]([CH3:36])[C@H:10]([O:19][C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[N:25]([C:29]1[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=1)[N:24]=[CH:23]2)[C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=1)=[O:7])(=[O:3])N>C(O)(=O)C>[F:35][C:32]1[CH:33]=[CH:34][C:29]([N:25]2[C:26]3[C:22](=[CH:21][C:20]([O:19][C@H:10]([C:11]4[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=4)[C@@H:9]([N:8]4[C:6](=[O:7])[CH2:5][NH:4][C:1]4=[O:3])[CH3:36])=[CH:28][CH:27]=3)[CH:23]=[N:24]2)=[CH:30][CH:31]=1参加物
3
反応条件
- 温度
- 120 °C
実験手順
2-(carbamoylamino)-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]acetamide (270, 141 mg, 0.29 mmol) was dissolved in acetic acid (3 mL). The reaction was heated at 120° C. with stirring for 20 h. The HOAc was evaporated and the product was purified by preparative HPLC.
後処理
- customThe HOAc was evaporated
- customthe product was purified by preparative HPLC
出典と根拠
- ORDレコード
- ord-2d4c05715e2349e7a7dc9ca064709663
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08143290B2
反応ノート
読み込み中…