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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288803Generated: October 27, 2026

4-Methylmorpholine → (R)-N-[(1,1-Dimethyl)ethoxycarbonyl]-S-methylcysteine N-methoxy-N-methylamide

https://huagongshe.com/reaction/2288803

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantBoc-cys(ME)-OHHCID 7018744—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
Product(R)-N-[(1,1-Dimethyl)ethoxycarbonyl]-S-methylcysteine N-methoxy-N-methylamideHCID 22942147—

Reaction Steps

A solution of Boc-S-methylcysteine (5 g), N,O-dimethylhydroxylamine hydrochloride (2.28 g) and N-hydroxybenzotriazole monohydrate (3.16 g) in tetrahydrofuran (60 ml) was treated with N-methylmorpholine at 0° C. under nitrogen. EDC (4.89 g) was added and the reaction was warmed to RT and stirred for 48 hours. The reaction mixture was concentrated in vacuo, to give a colourless residue which was partitioned between ethyl acetate (100 ml) and 10% citric acid (100 ml). The organic phase was washed with saturated sodium bicarbonate (70 ml) and brine (70 ml), dried (MgSO4), and evaporated to dryness in vacuo to give the title compound as a pale waxy solid (1.16 g, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090840
Source datasetuspto-grants-2000_07
ORD IDord-c8b01705618447b082dcc8c31c571ba6
Source noteuspto-grants-2000_07