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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791903Generated: November 4, 2026

Citric Acid → HCID 67506906, compound

https://huagongshe.com/reaction/1791903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67506856HCID 67506856—
SolventDimethylformamideHCID 6228—
ProductHCID 67506906HCID 67506906—

Reaction Steps

3-[(2S,4S)-1-tert-Butoxycarbonyl-4-(5-cyano-2-pyridyl)amino-2-pyrrolidinylcarbonyl]-1,3-thiazolidine [product of Example 58(1)] (305 mg) was dissolved in DMF (10 mL), and potassium tert-butoxide (93 mg) was added under ice cooling. After stirring the mixture for 10 min, benzyl bromide (94 μl) was added, and the mixture was stirred at room temperature for 3 days. 10% citric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed successively with saturated aqueous sodium hydrogencarbonate solution and brine, and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography to give 3-{(2S,4S)-4-[N-benzyl-N-(5-cyano-2-pyridyl)amino]-1-tert-butoxycarbonyl-2-pyrrolidinylcarbonyl}-1,3-thiazolidine (202 mg) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074794B2
Source datasetuspto-grants-2006_07
ORD IDord-a7776923fa85494fafd076a7edc9fc9f
Source noteuspto-grants-2006_07