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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-chloro-N-(5-fluoro-2-methylphenyl)acetamide | HCID 735852 | — |
| Reactant | 3,3-Dimethylhexahydro-3H-[1,3]oxazolo[3,4-a]pyrazine | HCID 21295645 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(5-fluoro-2-methylphenyl)-tetrahydro-3,3-dimethyl-3H-oxazolo[3,4-a]pyrazine-7(8H)-acetamide | HCID 21295689 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766125 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-381c5c99556c4f848281c9ccb2896c0f |
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| Source note | uspto-grants-1988_08 |
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