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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466003Generated: November 1, 2026

Water → 3-Carbamoylisoxazol-5-ylmethyl (-)-(R)-3-(naphth-2-yloxymethyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1466003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-MethylmorpholineHCID 7972—
Reactant(R)-3-(naphth-2-yloxymethyl)pyrrolidineHCID 26192527—
Reactant3-Carbamoylisoxazol-5-ylmethyl 4-nitrophenyl carbonateHCID 66660860—
SolventDichloromethaneHCID 6344—
Product3-Carbamoylisoxazol-5-ylmethyl (-)-(R)-3-(naphth-2-yloxymethyl)pyrrolidine-1-carboxylateHCID 6735091438.5%

Reaction Steps

0.21 g (0.92 mmol) of (R)-3-(naphth-2-yloxymethyl)-pyrrolidine is dissolved in 3.80 ml of dichloromethane and then 0.31 g (1.01 mmol) of 3-carbamoylisoxazol-5-ylmethyl 4-nitrophenyl carbonate and 0.15 ml (1.38 mmol) of N-methylmorpholine are added. The mixture is stirred at ambient temperature for 20 hours and then water is added to the reaction medium. After extraction of the aqueous phase with dichloromethane, the organic phases are successively washed three times with a 1M aqueous sodium hydroxide solution and then twice with a saturated aqueous ammonium chloride solution. After having dried the organic phases over sodium sulphate, they are filtered and the filtrate is evaporated to dryness. 0.14 g of the desired product is thus obtained in the form of a white solid after purification on a column of silica gel, elution being carried out with a dichloromethane/methanol mixture, and then taken up in isopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000010B2
Source datasetuspto-grants-2015_04
ORD IDord-a9c4d1cdfe134fa2be194f04004afc87
Source noteuspto-grants-2015_04