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HRID2213267

反应详情

EQUATION

反应方程式

HRID 2213267 的结构方程式

REACTANTS

反应物

2
结构：CNS(=O)(=O)Cc1ccc(N)cc1.Cl
HCID14234262

1-(4-Aminophenyl)-N-methylmethanesulfonamide--hydrogen chloride (1/1)

C8H13ClN2O2S

结构：CCOC=C1C(=O)Nc2ccc(-c3cnco3)cc21
HCID53832760

未命名化合物

PRODUCTS

生成物

1
结构：CNS(=O)(=O)Cc1ccc(NC=C2C(=O)Nc3ccc(-c4cnco4)cc32)cc1
HCID178486286

未命名化合物

收率 56%

PROCEDURE

实验过程

The title compound was prepared in 56% yield from ethoxymethylene-5-oxazol-5-yl-1,3-dihydro-indol-2-one and N-methyl-4-aminophenylmethanesulfonamide hydrochloride according to Procedure J: 1H NMR (DMSO-d6): δ 10.72 (d, 1H), 10.67 (s, 1H), 8.71 (d, 1H), 8.37 (s, 1H), 7.43–7.34 (m, 7H), 6.89 (m, 2H), 4.28 (s, 2H), 2.54 (d, 3H); APCI-MS m/z 409 (MH)−.