Tributylphenyltin → (+/-)-{9-[(4-chlorophenyl)thio]-6-fluoro-8-phenyl-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl}acetic acid
反応式
C[CH:2]([CH:6]1[C:10]2=[C:11]([S:20][C:21]3[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][CH:22]=3)[C:12]3[C:13](Br)=[CH:14][C:15]([F:18])=[CH:16][C:17]=3[N:9]2[CH2:8][CH2:7]1)[C:3]([O-:5])=[O:4].C([Sn](CCCC)(CCCC)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)CCC>>[Cl:27][C:24]1[CH:25]=[CH:26][C:21]([S:20][C:11]2[C:12]3[C:13]([C:33]4[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=4)=[CH:14][C:15]([F:18])=[CH:16][C:17]=3[N:9]3[CH2:8][CH2:7][CH:6]([CH2:2][C:3]([OH:5])=[O:4])[C:10]=23)=[CH:22][CH:23]=1参加物
3
実験手順
Starting from (+/−)-methyl{8-bromo-9-[(4-chlorophenyl)thio]-6-fluoro-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl}acetate (200 mg, 0.43 mmol) and tributyl(phenyl)stannane the title compound was synthesized following the procedures described in Example 42 and Step 10 of Example 7.
出典と根拠
- ORDレコード
- ord-8dfba1dfacd14e69aa6e7cddddc95563
- 出典データセット