Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063926Generated: November 1, 2026

Water → HCID 22276525, compound

https://huagongshe.com/reaction/1063926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant2-Methoxybenzoyl chlorideHCID 88969—
ReactantHCID 86588739HCID 86588739—
SolventChloroformHCID 6212—
ProductHCID 22276525HCID 22276525—

Reaction Steps

To a mixture of N-(2-tetrahydropyranyloxy-2-[7-(5-(4-chlorophenyl)-2-thienyl)-1,1-dioxoperhydro-1,4-thiazepin-7-yl]acetamide (90 mg) and pyridine (0.5 ml) in chloroform (3 ml) was added 2-methoxybenzoyl chloride (37 mg) and the mixture was stirred at ambient temperature for 3 hours. The mixture was pertitioned between water and chloroform. The organic layer was separated, washed with 5% citric acid water solution, water, saturated sodium bicarbonate solution and brine. To the reaction mixture were added 4N hydrogen chloride-ethyl acetate solution (0.5 ml), chloroform (1 ml) and methanol (1.5 ml) and the reaction mixture was stirred at ambient temperature for 30 minutes. After evaporation of solvent, the residue was purified by HPLC (0.1% trifluoroacetic acid in 20% acetonitrile-water ˜0.1% trifluoroacetic acid in 80% acetonitrile-water) to give N-hydroxy-2-[7-(5-(4-chlorophenyl)-2-thienyl)-4-(2-methoxybenzoyl)-1,1-dioxoperhydro-1,4-thiazepin-7-yl]acetamide (54 mg) as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967197B2
Source datasetuspto-grants-2005_11
ORD IDord-0d2daa5a34b04373b35a912865d27c31
Source noteuspto-grants-2005_11