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.[CH:22]([C:25]1[CH:26]=[CH:27][C:28]([O:34][CH3:35])=[C:29](B(O)O)[CH:30]=1)([CH3:24])[CH3:23].[CH2:36]([SH:39])[CH:37]=[CH2:38]>>[CH2:36]([S:39][CH2:12][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:27]3[CH:26]=[C:25]([CH:22]([CH3:24])[CH3:23])[CH:30]=[CH:29][C:28]=3[O:34][CH3:35])[CH:8]=2)[NH:3][C:2]([CH3:1])([CH3:21])[CH:11]=1)[CH:37]=[CH2:38]参加物
4
実験手順
Trifluoromethanesulfonic acid 2,2,4-trimethyl-1,2-dihydroquinolin-6-yl ester was coupled with 5-isopropyl-2-methoxyphenylboronic acid. Bromination and coupling reaction with allyl mercaptan gave 25 mg of the title compound.
出典と根拠
- ORDレコード
- ord-65bc0f663e534c029eaa0a76da58a392
- 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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