P-Toluenesulfonamide → Ethyl 2-(1-oxo-4-(tosylimino)-1,4-dihydronaphthalen-2-ylthio)acetate
反応式
[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)/[C:5](=N/S(C2SC=CC=2)(=O)=O)/[CH:4]=[C:3]1[S:21][CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24].[CH3:28][C:29]1[CH:34]=[CH:33][C:32]([S:35]([NH2:38])(=[O:37])=[O:36])=[CH:31][CH:30]=1>C1COCC1.Cl[Ti](Cl)(Cl)Cl>[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](=[N:38][S:35]([C:32]2[CH:31]=[CH:30][C:29]([CH3:28])=[CH:34][CH:33]=2)(=[O:37])=[O:36])[CH:4]=[C:3]1[S:21][CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24]参加物
5
実験手順
5.2.20 Ethyl 2-(1-oxo-4-(tosylimino)-1,4-dihydronaphthalen-2-ylthio)acetate (81) was prepared according to the procedure for 8a except using 4-methylbenzenesulfonamide, TiCl4.2THF and THF as solvent. The title compound 100.7 mg (46.9%) was obtained according to the workup procedure for 12a as a yellow solid, m.p.: ° C.
出典と根拠
- ORDレコード
- ord-dce73b7faefe44f3a10eb082648840b4
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08673910B2
反応ノート
読み込み中…