HRID1752530

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID263166

ethyl 5-(chloromethyl)-2-furoate

C8H9ClO3

结构：COC(=O)c1csc(CN2CCC(CNC(=O)c3n[nH]c4ccc(OC)cc34)CC2)n1

HCID89767420

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)c1ccc(CN2CCC(CNC(=O)c3n[nH]c4ccc(OC)cc34)CC2)o1

HCID89767412

未命名化合物

PROCEDURE

实验过程

Ethyl 5-{[4-({[(5-methoxy-1H-indazol-3-yl)carbonyl]amino}methyl) piperidin-1-yl]methyl}furan-2-carboxylate 23 was prepared, according to the procedure described for compound 7, starting from ethyl 5-(chloromethyl)furan-2-carboxylate. Yield: 290 mg, 71%.