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HRID1783571

反应详情

EQUATION

反应方程式

HRID 1783571 的结构方程式

REACTANTS

反应物

2
结构：C[C@@H]1CN(C(=O)c2ccccc2)CCN1
HCID7578227

(R)-1-Benzoyl-3-methylpiperazine

C12H16N2O

结构：O=C([O-])C(=O)c1c[nH]c2c(Cl)ccnc12.[K+]
HCID22893818

未命名化合物

PRODUCTS

生成物

1
结构：C[C@@H]1CN(C(=O)c2ccccc2)CCN1C(=O)C(=O)c1c[nH]c2c(Cl)ccnc12
HCID5495829

未命名化合物

PROCEDURE

实验过程

Precursor 5d, 1-benzoyl-3-(R)-methyl-4-[(7-chloro-4-azaindol-3-yl)-oxoacetyl]piperazine was prepared by the same method as Precursor 5a, starting from Potassium (7-chloro-4-azaindol-3-yl)-oxoacetate, Precursor 4e, and 1-benzoyl-3-(R)-methyl piperazine. MS m/z: (M+H)+ calcd for C21H20ClN4O3 411.12, found 411.04. HPLC retention time: 1.10 minutes (column A).