HRID1752521

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2049785

methyl 2-(chloromethyl)-3-furoate

C7H7ClO3

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：COC(=O)c1ccoc1CN1CCC(CNC(=O)c2n[nH]c3ccc(OC)cc23)CC1

HCID89767472

未命名化合物

PROCEDURE

实验过程

Methyl 2-{[4-({[(5-methoxy-1H-indazol-3-yl)carbonyl]amino}methyl) piperidin-1-yl]methyl}furan-3-carboxylate 14 was prepared, according to the procedure described for compound 7, using methyl 2-(chloromethyl)furan-3-carboxylate. Yield: 120 mg, 13%.