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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733992Generated: October 30, 2026

Hydrochloric Acid → HCID 9805201, compound

https://huagongshe.com/reaction/1733992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant5-Fluoro-2-methylbenzoyl chlorideHCID 2737383—
ReactantHCID 19699078HCID 19699078—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 9805201HCID 980520157.1%

Reaction Steps

To an ice bath cooled mixture of 345 mg of 6(2-chloro-4-aminobenzoyl)-1,4,5,6-tetrahydropyrazolo[3,4-d]thieno[3,2-b]azepine in 3.5 ml of methylene chloride is added 417 μl of triethylamine is added a solution of 432 mg of 2-methyl-5-fluorobenzoyl chloride in 1.5 ml of methylene chloride. The reaction mixture is stirred at room temperature for 18 hours under argon. An additional 40 ml of methylene chloride is added followed by 20 ml of water. The organic layer is washed with 20 ml each of 2N citric acid, 1M NaHCO3 and brine. The organic layer is dried (Na2SO4), filtered through hydrous magnesium silicate and the filtrate evaporated in vacuo to give a foam residue. To a solution of 800 mg of the preceding compound in 4 ml methanol and 4 ml of tetrahydrofuran is added 2.7 ml of 1N NaOH. The reactants are stirred at room temperature for 1.5 hours. The reaction mixture is neutralized with 1N HCl and evaporated in vacuo to a residue which is diluted with 50 ml of methylene chloride and water and then filtered. The collected solid is dried at 60° C. to give 275 mg of the desired product as an off-white solid, m.p. 310°-312° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532235
Source datasetuspto-grants-1996_07
ORD IDord-6f2471cfa22d408fa34bc4d03686d607
Source noteuspto-grants-1996_07