HRID506598

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2726447

N-(3-ethynylphenyl)acetamide

C10H9NO

HCID23665647

2-Methyl-2-propanol, potassium salt

C4H9KO

结构：CC(=O)Nc1cccc(-c2cc3cc([N+](=O)[O-])cnc3[nH]2)c1

HCID68462732

N-[3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)phenyl]acetamide

C15H12N4O3

PRODUCTS

生成物

结构：CC(=O)Nc1cccc(-c2cc3cc(NC(=O)OC(C)C)cnc3[nH]2)c1

HCID11530439

未命名化合物

PROCEDURE

实验过程

Was prepared analogously to example 9-2 starting from 3-(acetylamino)phenylacetylene. In the preparation of the intermediate N-[3-(5-nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)-phenyl]-acetamide by cyclization reaction an higher equimolar amount of base (Potassium tert-butoxide) as in Example 2-2 is needed: