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HRID1846844

反应详情

EQUATION

反应方程式

HRID 1846844 的结构方程式

REACTANTS

反应物

2
结构：O=Cc1oc(CNS(=O)(=O)c2ccccc2)cc(=O)c1OCc1ccccc1
HCID86725694

未命名化合物

结构：Cc1ccccc1S(=O)(=O)NCc1cc(=O)c(OCc2ccccc2)c(CO)o1
HCID86725701

未命名化合物

PRODUCTS

生成物

1
结构：Cc1ccccc1S(=O)(=O)NCc1cc(=O)c(OCc2ccccc2)c(C=O)o1
HCID86725702

未命名化合物

收率 66.92%

PROCEDURE

实验过程

N-(5-Benzyloxy-6-formyl-4-oxo-4H-pyran-2-ylmethyl)-2-methyl-benzenesulfonamide (11-02) (2.8 g, 66.92%) was synthesized as a white solid from N-(5-benzyloxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-2-methyl-benzenesulfonamide (10-02) (4.2 g, 10.12 mmol) following the procedure described for N-(5-benzyloxy-6-formyl-4-oxo-4H-pyran-2-ylmethyl)-benzenesulfonamide (11-01).