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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501565Generated: October 27, 2026

L-Hydroxyproline → (2S,3R)-1-(3-Chloro-4-cyano-2-methylphenylcarbamoyl)-3-hydroxypyrrolidine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/501565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-HydroxyprolineHCID 5810—
Reactant2-Chloro-4-isocyanato-3-methylbenzonitrileHCID 16731849—
ReactantMethyl (3R)-3-hydroxy-L-prolinateHCID 45082777—
SolventDichloromethaneHCID 6344—
Product(2S,3R)-1-(3-Chloro-4-cyano-2-methylphenylcarbamoyl)-3-hydroxypyrrolidine-2-carboxylic acid methyl esterHCID 5975428767.7%

Reaction Steps

To a solution of hydroxyproline compound 1F (493 mg, 3.40 mmol) in CH2Cl2 (15 mL) was added 4 Å molecular sieves (˜3.0 g), followed by isocyanate 23E (725 mg, 3.22 mmol), and the resulting mixture was stirred at rt overnight, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, 0.5% MeOH in EtOAc/hexane, 1:1) to afford the title compound (736 mg) as an off-white solid. HPLC column: YMC S-5 C18 (4.6×50 mm), 0% to 100% B, 4 min gradient, 1 min hold (A=90% H2O-10% CH3CN-0.1% TFA and B=10% H2O-90% CH3CN-0.1% TFA), flow rate at 4 mL/min, UV detection at 220 nm, 1.57 min retention time (100%); MS (ES) m/z 338 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772267B2
Source datasetuspto-grants-2010_08
ORD IDord-46bb7aecb6b6449bbdae976364582357
Source noteuspto-grants-2010_08