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HRID1783570

反应详情

EQUATION

反应方程式

HRID 1783570 的结构方程式

REACTANTS

反应物

2
反应SMILES：O=C(c1ccccc1)N1CCNCC1
HCID762654

1-Benzoylpiperazine

C11H14N2O

反应SMILES：COc1cnc(Cl)c2[nH]cc(C(=O)C(=O)[O-])c12.[K+]
HCID22893812

未命名化合物

PRODUCTS

产物

1
反应SMILES：COc1cnc(Cl)c2[nH]cc(C(=O)C(=O)N3CCN(C(=O)c4ccccc4)CC3)c12
HCID5495838

未命名化合物

PROCEDURE

实验过程

Precursor 5b, 1-benzoyl-4-[(7-chloro-4-methoxy-6-azaindol-3-yl)-oxoacetyl]piperazine was prepared by the same method as Precursor 5a starting from Potassium (7-chloro-4-methoxy-6-azaindol-3-yl)-oxoacetate, Precursor 4d, and 1-benzoylpiperazine. MS m/z: (M+H)+ calcd for C21H20ClN4O4: 427.12; found 427.12. HPLC retention time: 1.28 minutes (column A).