5-(4-(Trifluoromethyl)phenyl)oxazole → 4-(4-Trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindine
反応式
F[C:2]1[CH:3]=[C:4]([C:12]2[C:20]3[CH2:19][CH2:18][CH2:17][C:16]=3[CH:15]=[N:14][CH:13]=2)[CH:5]=[CH:6][C:7]=1[C:8]([F:11])([F:10])[F:9].FC(F)(F)C1C=CC(C2OC=NC=2)=CC=1>>[F:11][C:8]([F:9])([F:10])[C:7]1[CH:2]=[CH:3][C:4]([C:12]2[C:20]3[CH2:19][CH2:18][CH2:17][C:16]=3[CH:15]=[N:14][CH:13]=2)=[CH:5][CH:6]=1参加物
3
実験手順
In analogy to the procedure described for the preparation of 4-(3-fluoro-4-trifluoromethyl-phenyl)-6,7-dihydro-5H-[2]pyrindine (intermediate A-14 [B], batch approach), replacing 5-(3-fluoro-4-(trifluoromethyl)phenyl)-oxazole with 5-(4-trifluoromethyl-phenyl)-oxazole (CAS[87150-14-9]). The title compound was obtained as a light brown oil in 32% yield. MS: 264.1 (M+H)+.
出典と根拠
- ORDレコード
- ord-1ce009e69cd24730a21472edc7cf6427
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09187429B2
反応ノート
読み込み中…