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HRID1019887

反应详情

EQUATION

反应方程式

HRID 1019887 的结构方程式

REACTANTS

反应物

3
结构：CC(C)(C)OC(=O)NC1CCN(CCO)CC1
HCID45076484

tert-Butyl [1-(2-hydroxyethyl)piperidin-4-yl]carbamate

C12H24N2O3

结构：O=C1CSc2cc(Cl)c(C(=O)O)cc2N1
HCID59560634

未命名化合物

结构：COc1cnc2ccc(Cl)nc2c1
HCID71463962

2-Chloro-7-methoxy-1,5-naphthyridine

C9H7ClN2O

PRODUCTS

生成物

1
结构：COc1cnc2ccc(OCCN3CCC(NC(=O)c4cc5c(cc4Cl)SCC(=O)N5)CC3)nc2c1
HCID46852382

未命名化合物

PROCEDURE

实验过程

The title compound is prepared as an off-white lyophilizated powder following Scheme 1 and in analogy to Example 1 using 2-chloro-7-methoxy-[1,5]naphthyridine, [1-(2-hydroxy-ethyl)-piperidin-4-yl]-carbamic acid tert-butyl ester and 7-chloro-3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid as starting materials.