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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255984Generated: November 2, 2026

Triethylamine → HCID 21467149, compound

https://huagongshe.com/reaction/2255984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Fluoro-2-methylbenzoyl chlorideHCID 2779240—
ReactantHCID 21467138HCID 21467138—
SolventDichloromethaneHCID 6344—
ProductHCID 21467149HCID 2146714972%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654297
Source datasetuspto-grants-1997_08
ORD IDord-36515d6b372a4b55b41edc495ba6e3fc
Source noteuspto-grants-1997_08