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HRID987544

反应详情

EQUATION

反应方程式

HRID 987544 的结构方程式

REACTANTS

反应物

2
结构：COc1ncc(OC)c2c(C(=O)C(=O)N3CCN(C(=O)c4ccccc4)CC3C)c[nH]c12
HCID22476268

未命名化合物

结构：COc1ncc(OC)c2c(C(=O)C(=O)[O-])c[nH]c12.[K+]
HCID22893810

未命名化合物

PRODUCTS

生成物

1
结构：COc1cnc(OC)c2[nH]ccc12
HCID22476295

4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridine

C9H10N2O2

PROCEDURE

实验过程

Compound 5ap, {circle around (R)}N-(benzoyl)-3-methyl-N′-[(4,7-dimethoxy-6-azaindol-3-yl)-oxoacetyl]piperazine (white solid) was prepared using the same method used to prepare compound 5a except that Potassium (4,7-dimethoxy-6-azaindol-3-yl)-oxoacetate was used as the starting material. MS m/z: (M+H)+ calcd for C23H25N4O5: 437.18; found 437.24. HPLC retention time: 1.37 minutes (column B).