反应详情

A solution of 2-(4-aminophenyl)-1-ethyl-6-methoxy-1H-indole-3-carbonitrile, prepared by example 1Ga step B, (0.82 mg, 2.82 mmol), in pyridine (10 mL) was treated dropwise with chloroethyl sulfonylchloride (0.38 mL, 3.66 mmol) at room temperature. After stirring for 4 h, the reaction mixture was quenched with ice-water and enough 6N HCl was added until the pH was lowered to 2. The suspension was extracted with hot EtOAc (3×). The organic phases were then washed sequentially with 1N HCl, H2O and saturated NaCl and dried and concentrated to give ethenesulfonic acid [4-(3-cyano-1-ethyl-6-methoxy-1H-indol-2-yl)-phenyl] amide as a pale orange solid which was used directly in the next step without further purification.

1. customthe reaction mixture was quenched with ice-water and enough 6N HCl
2. additionwas added until the pH
3. extractionThe suspension was extracted with hot EtOAc (3×)
4. washThe organic phases were then washed sequentially with 1N HCl, H2O and saturated NaCl
5. customdried
6. concentrationconcentrated