反応式
[CH3:1][C:2]1([CH3:21])[CH:11]=[C:10]([CH3:12])[C:9]2[C:4](=[CH:5][CH:6]=[C:7](OS(C(F)(F)F)(=O)=O)[CH:8]=2)[NH:3]1.[C:22]1([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[C:23](B(O)O)=[CH:24][CH:25]=[CH:26][CH:27]=1.[CH2:37]([SH:40])[CH:38]=[CH2:39]>>[CH2:37]([S:40][CH2:12][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:27]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)[CH:8]=2)[NH:3][C:2]([CH3:1])([CH3:21])[CH:11]=1)[CH:38]=[CH2:39]参加物
4
実験手順
Trifluoromethanesulfonic acid 2,2,4-trimethyl-1,2-dihydroquinolin-6-yl ester was coupled with 2-biphenylboronic acid. Bromination and coupling reaction with allyl mercaptan gave 13 mg of the title compound.
出典と根拠
- ORDレコード
- ord-b66c054f415e4270aa2da203bb102950
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06858627B2
関連ノート
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