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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475338Generated: October 30, 2026

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

https://huagongshe.com/reaction/475338

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 M in 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 numberUS08637546B2
Source datasetuspto-grants-2014_01
ORD IDord-7188a4212ca048b882b5c2a78c7f134d
Source noteuspto-grants-2014_01