Benzenesulfonyl chloride → 1-(Phenylsulfonyl)-3,4-dihydropyrrolo[4,3,2-de]isoquinolin-5(1H)-one

反応式

[C:1]1([S:7](Cl)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+].[NH:13]1[C:23]2[C:24]3[C:15]([CH2:16][NH:17][C:18](=[O:25])[C:19]=3[CH:20]=[CH:21][CH:22]=2)=[CH:14]1>C(Cl)Cl>[C:1]1([S:7]([N:13]2[C:23]3[C:24]4[C:15]([CH2:16][NH:17][C:18](=[O:25])[C:19]=4[CH:20]=[CH:21][CH:22]=3)=[CH:14]2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

参加物

実験手順

Benzenesulfonyl chloride (140 mg, 0.79 mmol), NBu4HSO4 (24 mg, 0.07 mmol) and 4M aq. NaOH (2 mL) were, in that order, added to 3,4-Dihydropyrrolo[4,3,2-de]isoquinolin-5(1H)-one, Intermediate 1 (124 mg, 0.72 mmol) in DCM (10 mL). The reaction was stirred at room temperature for 2 h and then extracted with water and DCM (×2). The product seems to be only partially soluble in DCM and some solid material in the water layer was filtered off and added to the DCM layer, which was concentrated and dried to give 227 mg of the title compound, as a light brown solid. MS m/z 313 [M+H]+.