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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829111Generated: November 1, 2026

Citric Acid → HCID 67506906, compound

https://huagongshe.com/reaction/1829111

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 numberUS07060722B2
Source datasetuspto-grants-2006_06
ORD IDord-ac87bdf35a9a488abfb0430de2c6bdd1
Source noteuspto-grants-2006_06