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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361787Generated: October 26, 2026

Ammonia → N-BOC-b-cyclohexylalanine amide

https://huagongshe.com/reaction/361787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant(2S)-2-(((tert-butoxy)carbonyl)amino)-3-cyclohexylpropanoic acidHCID 10588189—
SolventMethanolHCID 887—
ProductN-BOC-b-cyclohexylalanine amideHCID 86584122—

Reaction Conditions

Temperature-20 °C

Reaction Steps

N-[N-[N-(4-(piperidin-4-yl)butanoyl)-N-ethylglycyl]aspartyl]-L-β-cyclohexyl alanine amide ##STR17##A. N-BOC-β-cyclohexylalanine (2.0 g.) and triethyl amine (1.03 ml) aredissolved together in THF (100 ml) and the solution cooled to -20° C. Isobutyl chloroformate (1.06 ml) is added and the solution stirred at -20° C. for about 30 minutes. A saturated solution of ammonia in methanol (20 ml) is added and the solution allowed to warm to room temperature and stirred at room temperature for about 18 hours. The solution is evaporated in vacuo and the residue dissolved in ethyl acetate. The ethyl acetate solution is washed with water, 5% HCl, saturated sodium bicarbonate solution, water, brine, dried over sodium sulfate, filtered and evaporated in vacuo to give N-BOC-β-cyclohexylalanine amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866685
Source datasetuspto-grants-1999_02
ORD IDord-48ecf49b4a9a4c6eae2cd1a4652d58ff
Source noteuspto-grants-1999_02