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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477450생성일: 2026년 10월 25일

5-Aminoimidazole-4-carboxamide hydrochloride → 4-(2,5-Dichlorophenyl)imidazo[1,5-a]pyrimidine-8-carboxamide

https://huagongshe.com/reaction/477450

반응식

참여 물질

역할이름HCID투입량
반응물5-Aminoimidazole-4-carboxamide hydrochlorideHCID 66146—
반응물Sodium BicarbonateHCID 516892—
반응물2',5'-Dichloro-3-dimethylaminoacrylophenoneHCID 2806206—
반응물Methylenechloride HexaneHCID 21226440—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
생성물4-(2,5-Dichlorophenyl)imidazo[1,5-a]pyrimidine-8-carboxamideHCID 1467747374.3%

반응 단계

A stirred mixture of 5.2 g of 4-amino-5-imidazolecarboxamide hydrochloride and 10.0 g of 2',5'-dichloro-3-dimethylaminoacrylophenone (prepared as described in Example 4) in 80 ml of glacial acetic acid was heated at reflux for 4 hours. Evaporation in vacuo gave a dark oil which was dissolved in dichloromethane and treated with saturated sodium bicarbonate. The organic layer was separated, washed with water then dried over anhydrous sodium sulfate. The dichloromethane solution was passed through a short column of hydrous magnesium silicate. Evaporation of the eluate gave a semi-solid which was treated with hot dichloromethane-hexane to give a yellow precipitate which was collected by filtration and dried to give 7.3 g of the product of the example, mp 230°-234° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04888345
출처 데이터셋uspto-grants-1989_12
ORD IDord-b4225ec8f3b146fb9fffca1c71b90481
출처 메모uspto-grants-1989_12