Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Fluoro-2-methylbenzoyl chloride | HCID 2779240 | — |
| Reactant | HCID 21467138 | HCID 21467138 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21467149 | HCID 21467149 | 72% |
Reaction Steps
To a mixture of 287 mg of 4,5,6,7-tetrahydro-4-(4-aminobenzoyl)-8H-thieno[3,2-b]azepin-8-one in 3 ml of methylene chloride is added 209 μl of triethylamine which is cooled to 0° C. is added 207.1 mg of 2-methyl-3-fluorobenzoyl chloride. The cooling bath is removed and the reaction mixture stirred at room temperature under argon for 18 hours. An additional 50 ml of methylene chloride and 20 ml of water is added and the separated organic layer washed with 2N citric acid, 1M NaHCO3 and brine. The organic layer is dried with Na2SO4 and passed through a short pad of hydrous magnesium silicate and the filtrate evaporated in vacuo to a white foam which is crystallized from ethyl acetate-hexane to give 305 mg of the desired product as a white solid, 200°-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05654297 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-36515d6b372a4b55b41edc495ba6e3fc |
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| Source note | uspto-grants-1997_08 |
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