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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35332생성일: 2026년 10월 24일

Triethylamine → N-(2,6-dimethylphenyl)hexahydro-3,3-dimethyl-2-(1-methylethyl)-1-oxoimidazo[1,5-a]pyrazine-7(8H)-acetamide

https://huagongshe.com/ko/reaction/35332

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Chloro-N-(2,6-dimethylphenyl)acetamideHCID 70798—
반응물hexahydro-3,3-dimethyl-2-(1-methylethyl)imidazo[1,5-a]pyrazin-1(5H)-oneHCID 21295654—
용매DimethylformamideHCID 6228—
생성물N-(2,6-dimethylphenyl)hexahydro-3,3-dimethyl-2-(1-methylethyl)-1-oxoimidazo[1,5-a]pyrazine-7(8H)-acetamideHCID 1423024272.7%

반응 조건

온도75 °C

반응 단계

A mixture of 8.2 parts of 2-chloro-N-(2,6-dimethylphenyl)acetamide, 7.2 parts of hexahydro-3,3-dimethyl-2-(1-methylethyl)imidazo[1,5-a]pyrazin-1(5H)-one, 7 parts of N,N-diethylethanamine and 54 parts of N,N-dimethylformamide was stirred and heated for 3 hours at 75° C. After cooling to 0° C., the precipitate was filtered off and the filtrate was evaporated. The residue was dissolved in 300 parts of trichloromethane. This solution was washed with 50 parts of water, dried, filtered and evaporated. The residue was triturated in 2,2'-oxybispropane. After cooling to 0° C., the product was filtered off and dried, yielding 9.2 parts (72.7%) of N-(2,6-dimethylphenyl)hexahydro-3,3-dimethyl-2-(1-methylethyl)-1-oxoimidazo[1,5-a]pyrazine-7(8H)-acetamide; mp. 155° C. (intermediate 101).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766125
출처 데이터셋uspto-grants-1988_08
ORD IDord-aefb654b87b7431f99ffecb3fefb8341
출처 메모uspto-grants-1988_08