Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35333Generated: October 29, 2026

Triethylamine → N-(5-fluoro-2-methylphenyl)-tetrahydro-3,3-dimethyl-3H-oxazolo[3,4-a]pyrazine-7(8H)-acetamide

https://huagongshe.com/reaction/35333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-chloro-N-(5-fluoro-2-methylphenyl)acetamideHCID 735852—
Reactant3,3-Dimethylhexahydro-3H-[1,3]oxazolo[3,4-a]pyrazineHCID 21295645—
SolventDimethylformamideHCID 6228—
ProductN-(5-fluoro-2-methylphenyl)-tetrahydro-3,3-dimethyl-3H-oxazolo[3,4-a]pyrazine-7(8H)-acetamideHCID 21295689—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 6.6 parts of 2-chloro-N-(5-fluoro-2-methylphenyl)acetamide, 5 parts of hexahydro-3,3-dimethyl-3H-oxazolo[3,4-a]pyrazine, 6.1 parts of N,N-diethylethanamine and 67.5 parts of N,N-dimethylformamide was stirred and heated for 8 hours at about 70° C. After cooling overnight to room temperature, the reaction mixture was evaporated. The residue was dissolved in trichloromethane. The solution was washed with water, dried, filtered and evaporated, yielding 8.5 parts of N-(5-fluoro-2-methylphenyl)-tetrahydro-3,3-dimethyl-3H-oxazolo[3,4-a]pyrazine-7(8H)-acetamide as an oily residue (intermediate 121).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766125
Source datasetuspto-grants-1988_08
ORD IDord-381c5c99556c4f848281c9ccb2896c0f
Source noteuspto-grants-1988_08