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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246420Generated: November 4, 2026

Triethylamine → HCID 68685886, compound

https://huagongshe.com/reaction/2246420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantL-Glutamic acid, N-((1,1-dimethylethoxy)carbonyl)-, 5-(phenylmethyl) esterHCID 83589—
ReactantDioxane methylene chlorideHCID 18626912—
ReactantPyrrolidine-2-carbonitrile--hydrogen chloride (1/1)HCID 21864982—
ProductHCID 68685886HCID 6868588680%

Reaction Steps

t-Butoxycarbonyl-L-glutamic acid 5-benzyl ester (A) (0.65 g, 2 mmol) and N-hydroxysuccinimide (HOSu, 0.23 g, 2 mmol) were dissolved in 6 ml of CH2Cl2/4-dioxane (2/1). The solution was cooled in an ice-water bath and dicyclohexylcarbodimide (DCC, 0.45 g, 2.2 mmol) was added with stirring. The reaction mixture was stirred at room temperature for 1 hour and then pyrrolidine-2-carbonitrile hydrochloride (B) (0.27 g, 2 mmol) and triethylamine (Et3N, 0.22 g, 2.2 mmol) were added. After 4 hours at room temperature, DCC was removed by filtration and washed by CH2Cl2. The filtrate and washings were combined and washed with 10% aqueous citric acid and then saturated aqueous NaHCO3, dried over MgSO4, and concentrated in vacuo. Further purification by flash column chromatography (eluted with 5/4/1 hexane/CH2Cl2/EA) afforded compound (C) (80%) as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687504B2
Source datasetuspto-grants-2010_03
ORD IDord-c3a817eabb6e4dbd88219ca877b3ceb2
Source noteuspto-grants-2010_03