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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892609Generated: October 30, 2026

Thiazolidine → HCID 53784898, compound

https://huagongshe.com/reaction/892609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidineHCID 10444—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 28789692HCID 28789692—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 53784898HCID 53784898—

Reaction Conditions

Temperature-25 °C

Reaction Steps

N-[(2-Oxo-1-pyrrolidinyl)acetyl]-L-proline as prepared in Example 1-B) (623 mg) was suspended in a mixture of methylene chloride (3 ml) and DMF (5 ml), to which were added HOBt (530 mg) and thiazolidine (0.21 ml). The mixture was cooled to -25° C. and DCC (588 mg) was added thereto. The mixture was stirred at a temperature of -25°-0° C. for 3 hours and at room temperature for 12 hours. The precipitated dicyclohexylurea was filtered off, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (chloroform-methanol) to give 468 mg of 3-{N-[(2-oxo-1-pyrrolidinyl)acetyl]-L-prolyl}thiazolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118811
Source datasetuspto-grants-1992_06
ORD IDord-6be11c1451834a5381b894b980be3703
Source noteuspto-grants-1992_06