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HRID 1605作成日:2026年10月24日

Acetic Acid → ethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate

https://huagongshe.com/ja/reaction/1605

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Ammonium AcetateHCID 517165—
反応物Diethyl 1-(6-chloro-1-oxoindan-2-yl)imidazole-2,4-dicarboxylateHCID 19691073—
溶媒AcetoneHCID 180—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
生成物ethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylateHCID 1969106761.7%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726175
出典データセットuspto-grants-1998_03
ORD IDord-e4f280544c164e7781c5e91559bf59d4
出典メモuspto-grants-1998_03