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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732290Generated: October 26, 2026

Ammonia → {(S)-2-carbamoylmethyl-4-methylpentyl)carbamic acid methyl ester

https://huagongshe.com/reaction/732290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTetrahydrofuranHCID 8028—
ReactantSodiumHCID 5360545—
ReactantMethyl ((S)-4-Methyl-2-[2-oxo-2-[[(S)-1-phenylethyl]amino]ethyl]pentyl]carbamateHCID 59832562—
SolventWaterHCID 962—
Product{(S)-2-carbamoylmethyl-4-methylpentyl)carbamic acid methyl esterHCID 5983256460.5%

Reaction Steps

A 2 l, four-necked flask, equipped with a mechanical stirrer, thermometer pocket and a liquid ammonia inlet, was charged with {(S)-4-methyl-2-[((S)-1-phenylethylcarbamoyl)-methyl ]pentyl}carbamic acid methyl ester (26) (25 g, 0.078 mole), tetrahydrofuran (175 ml), and water (25 ml). The reaction mixture was cooled to −40° to −60° C. and liquid ammonia (1000 ml) was added followed by addition of small pieces of sodium metal (7.2 g). The resultant reaction mixture was stirred vigorously for 4-10 hours until the ammonia had evaporated. Water (100 ml) was added to the reaction mass under N2 atmosphere at 5°-10° C., followed by separating the phases. The organic layer was separated and dried over anhydrous sodium sulphate and the solvent was stripped off. The residue was crystallized from diisopropyl ether to get 10.2 g (60% yield) of {(S)-2-carbamoylmethyl-4-methylpentyl)carbamic acid methyl ester with purity of 73% as measured by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07586005B2
Source datasetuspto-grants-2009_09
ORD IDord-b48100371583410784340d34bc81a124
Source noteuspto-grants-2009_09