反応式
[C:1]([C:3]1[CH:30]=[CH:29][C:6]([CH2:7][N:8]2[C:13]([CH3:14])=[C:12]([C:15]3[CH:20]=[CH:19][CH:18]=[C:17]([C:21](F)([F:23])[F:22])[CH:16]=3)[C:11](=[O:25])[C:10]([C:26]([OH:28])=[O:27])=[CH:9]2)=[CH:5][CH:4]=1)#[N:2].F[CH:32](F)C1C=CC=CC=1B(O)O.BrC1C(=O)C(C(O)=O)=CN(CC2C=CC(C#N)=CC=2)C=1C.BrC1C(=O)C(C(O)=O)=CN(C(C2C=CC(C#N)=CC=2)C)C=1C>>[C:1]([C:3]1[CH:30]=[CH:29][C:6]([CH:7]([N:8]2[C:13]([CH3:14])=[C:12]([C:15]3[CH:20]=[CH:19][CH:18]=[C:17]([CH:21]([F:23])[F:22])[CH:16]=3)[C:11](=[O:25])[C:10]([C:26]([OH:28])=[O:27])=[CH:9]2)[CH3:32])=[CH:5][CH:4]=1)#[N:2]参加物
5
反応物 4
生成物 1
実験手順
Preparation 3 is prepared following the procedure described for preparation 1d, substituting 3-(trifluoromethyl)phenylboronic acid with 2-(difluoromethyl)phenylboronic acid and substituting preparation 1c with preparation 2b as starting material. ESI mass spectrum: [M+H]+=409; Retention time HPLC: 1.00 min (Z018_S04).
後処理
- customPreparation 3
- customis prepared
- custom1.00 min (Z018_S04)
出典と根拠
- ORDレコード
- ord-ee70be4464134afeb5a8e4b8bf19bd9c
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09102624B2
関連ノート
読み込み中…