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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350752Generated: October 29, 2026

Hydrochloric Acid → HCID 21088584, compound

https://huagongshe.com/reaction/350752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThiazolidineHCID 10444—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantHOAtHCID 181649—
ReactantHCID 21088585HCID 21088585—
SolventDimethylformamideHCID 6228—
ProductHCID 21088584HCID 2108858446.1%

Reaction Steps

A mixture of thiazolidine (145 mg), 3-{3-[2-(1H-benzoimidazol-1-yl)-4-(4-chlorophenyl}-5-oxazolyl]propionic acid (300 mg), 1-hydroxy-7-aza-1H-1,2,3-benzotriazole (222 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (253 mg) and N,N-dimethylformamide (1 ml) was stirred overnight at room temperature. To the reaction mixture was added 0.1N aqueous hydrochloric acid solution (16 ml) and the reaction mixture was extracted with ethyl acetate (5 ml). The organic layer was concentrated, introduced into preparative HPLC and purified to give 3-{3-[2-(1H-benzoimidazol-1-yl)-4-(4-chlorophenyl)-5-oxazolyl]propanoyl}thiazolidine (165 mg, 46%). Recrystallization from ethyl acetate-hexane gave yellow prism crystals. melting point: 125–126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183276B2
Source datasetuspto-grants-2007_02
ORD IDord-b97852ece6334054b409144ca3f3fadb
Source noteuspto-grants-2007_02