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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35332Generated: October 26, 2026

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

https://huagongshe.com/reaction/35332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-N-(2,6-dimethylphenyl)acetamideHCID 70798—
Reactanthexahydro-3,3-dimethyl-2-(1-methylethyl)imidazo[1,5-a]pyrazin-1(5H)-oneHCID 21295654—
SolventDimethylformamideHCID 6228—
ProductN-(2,6-dimethylphenyl)hexahydro-3,3-dimethyl-2-(1-methylethyl)-1-oxoimidazo[1,5-a]pyrazine-7(8H)-acetamideHCID 1423024272.7%

Reaction Conditions

Temperature75 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766125
Source datasetuspto-grants-1988_08
ORD IDord-aefb654b87b7431f99ffecb3fefb8341
Source noteuspto-grants-1988_08