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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747771Generated: October 30, 2026

Benzoic Acid → benzyl (3R)-4-(5-cyano-2-iodophenoxy)-3-[4-(pyrrolidine-1-carbonyl)benzoylamino]butyrate

https://huagongshe.com/reaction/747771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(1R)-1-benzyloxycarbonylmethyl-2-(5-cyano-2-iodophenoxy)ethylammonium chlorideHCID 86760714—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productbenzyl (3R)-4-(5-cyano-2-iodophenoxy)-3-[4-(pyrrolidine-1-carbonyl)benzoylamino]butyrateHCID 86760715—

Reaction Steps

2.0 g (4.23 mmol) of (1R)-1-benzyloxycarbonylmethyl-2-(5-cyano-2-iodophenoxy)ethyl ammonium chloride, 1.02 g (4.65 mmol) of 4-pyrrolidine-1-carbonyl)benzoic acid, 630 mg (4.65 mmol) of 1-hydroxybenzotriazole, and 1.30 ml (9.31 mmol) of triethylamine were dissolved in 40 ml of dichloromethane, and 890 mg (4.65 mmol) of 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride was added thereto and stirred under cooling with ice for 10 minutes and then at room temperature for 18 hours. The reaction was stopped by adding water, and the title compound was obtained in an ordinary manner by treatment with dichloromethane as the extractant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396844B1
Source datasetuspto-grants-2008_07
ORD IDord-668648b39abc4945a20eb03e2dccf5a3
Source noteuspto-grants-2008_07