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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642656Generated: November 2, 2026

Ammonia → N-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-prolinamide

https://huagongshe.com/reaction/1642656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-prolineHCID 71367827—
SolventTetrahydrofuranHCID 8028—
ProductN-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-prolinamideHCID 86592933—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of N-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-proline (2.83 mmol) and N-methyl morpholine (0.39 mL, 3.50 mmol) in THF (15 mL) was added isobutyl chloroformate (0.42 mL, 3.25 mmol). The resulting cloudy white mixture was stirred at 0° C. for 30 minutes followed by the addition of a solution of ammonia (0.5 Min dioxane, 10.0 mL, 5.0 mmol). The solution was allowed to warm to room temperature and stirred for 16 hours. The reaction mixture was diluted by the addition of 1 M HCl (100 mL), and extracted with ethyl acetate (3×100 mL). The combined organic layers were dried (sodium sulfate), filtered, and concentrated to provide the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119664B2
Source datasetuspto-grants-2012_02
ORD IDord-e4dec92b07c849388ece3f70cecb05af
Source noteuspto-grants-2012_02