反応式
[C:1]([OH:7])([C:3]([F:6])([F:5])[F:4])=[O:2].C(O[C:13](=O)[NH:14][CH:15]1C[N:17]([CH:19]2[CH2:24][CH2:23][CH:22]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[CH2:21][CH2:20]2)[CH2:16]1)(C)(C)C>>[OH:7][C:1]([C:3]([F:6])([F:5])[F:4])=[O:2].[C:25]1([CH:22]2[CH2:23][CH2:24][CH:19]([NH:17][CH:16]3[CH2:13][NH:14][CH2:15]3)[CH2:20][CH2:21]2)[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1参加物
3
実験手順
The title compound was prepared as colorless oil from the TFA de-protection of [1-(4-phenyl-cyclohexyl)-azetidin-3-yl]-carbamic acid tert-butyl ester (as prepared in the previous step) using the procedure described in Step E of Example 1.
後処理
- customas prepared in the previous step)
出典と根拠
- ORDレコード
- ord-5a3ca7c057f6405d837d155fb0caf671
- 出典データセット
- uspto-grants-2013_08
- 特許番号
- US08513229B2
関連ノート
読み込み中…