Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385128Generated: October 29, 2026

Thiazolidine → HCID 68108646, compound

https://huagongshe.com/reaction/385128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidineHCID 10444—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 68108180HCID 68108180—
SolventDichloromethaneHCID 6344—
ProductHCID 68108646HCID 68108646—

Reaction Steps

5-(1,1-dioxo-2,3-dihydro-1,3-benzothiazole-3-carbonyl)-2-methoxy-3-trifluoromethylbenzoic acid (277 mg) was dissolved in dichloromethane (3 mL), thiazolidine (0.10 mL) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (238 mg) were added to the solution, and then the mixture was stirred at room temperature for 19 hours. The solvent was distilled off under reduced pressure and 1N hydrochloric acid was added and then the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (138 mg) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-ba8599c8d94144c0b5b355801e683d67
Source noteuspto-grants-2013_02