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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36509Generated: October 25, 2026

4-Methylmorpholine → N-benzyloxycarbonyl-L-leucinamide

https://huagongshe.com/reaction/36509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantLeucine, N-carboxy-, N-benzyl ester, L-HCID 74840—
ReactantAmmonia methanolHCID 21705897—
SolventDichloromethaneHCID 6344—
ProductN-benzyloxycarbonyl-L-leucinamideHCID 69952024—

Reaction Steps

To a solution of N-[(phenylmethoxy)carbonyl]-L-leucine (3 g., 11.3 mmol.) in 60 mL of methylene chloride at -20° under argon was added N-methylmorpholine (1.24 mL, 11.3 mmol.) followed by isobutylchloroformate (1.47 mL, 11.3 mmol.). The resulting suspension was stirred at -20° C. for 15 minutes at which time a solution of ammonia/methanol (about 5.6M, 20 mL, 113 mmol.) was added. After 30 minutes at -20° C., the reaction was quenched with water and warmed to room temperature. The layers were separated and the aqueous layer was extracted with methylene chloride (2 x). The combined organic extracts were dried (MgSO4) and evaporated to give 2.82 g. of the title A compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05414013
Source datasetuspto-grants-1995_05
ORD IDord-3d848cf5661e4511be75349638e4c970
Source noteuspto-grants-1995_05