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HRID1443880

反应详情

EQUATION

反应方程式

HRID 1443880 的结构方程式

REACTANTS

反应物

2
结构：CC1CN(C(=O)c2ccccc2)CCN1
HCID10726887

1-BENZOYL-3-METHYLPIPERAZINE

C12H16N2O

结构：COc1ccc(-c2ccnc3c(C(=O)C(=O)[O-])c[nH]c23)cc1.[K+]
HCID59693981

1H-Pyrrolo[3,2-b]pyridine-3-acetic acid, 7-(4-methoxyphenyl)-α-oxo-, potassium salt (1:1)

C16H11KN2O4

PRODUCTS

生成物

1
结构：COc1ccc(-c2ccnc3c(C(=O)C(=O)N4CCN(C(=O)c5ccccc5)C[C@H]4C)c[nH]c23)cc1
HCID5280226

未命名化合物

PROCEDURE

实验过程

Example 67, 1-benzoyl-3-(R)-methyl-4-[(7-(4-methoxyphenyl)-4-azaindol-3-yl)oxoacetyl]piperazine was prepared from potassium 7-(4-methoxyphenyl)-4-azaindole-3-glyoxylate and the corresponding 1-benzoyl-3-methylpiperazine according to the above general procedure. MS m/z: (M+H)+ Calc'd for C28H27N4O4: 483.20; found 483.16. HPLC retention time: 1.28 minutes (column A).