反应 #1701
ord-e4f280544c164e7781c5e91559bf59d4
反应方程式
diethyl 1-(6-chloro-1-oxoindan-2-yl)imidazole-2,4-dicarboxylate
ammonium acetate
acetic acid
→
ethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate
收率 61.7%
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1洗涤After washing the precipitate with water
- 2其他with methyl ethyl ketone, the solid obtained
实验过程
The procedure is as in Example 1 but starting from 5 g of diethyl 1-(6-chloro-1-oxoindan-2-yl)imidazole-2,4-dicarboxylate, 118 g of ammonium acetate and 190 ml of acetic acid. After washing the precipitate with water and then with methyl ethyl ketone, the solid obtained is first of all ground in acetonitrile and then in methanol and finally in acetone to obtain 2.7 g of ethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate in the form of a brown solid melting above 260° C. (analysis % calculated C: 58.28, H: 3.67, Cl: 10.75, N: 12.74; % found C: 58.6, H: 3.4, Cl: 10.4, N: 13.1).