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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491629Generated: October 26, 2026

4-Methylmorpholine → (1,1-dimethylethyl) (S)-[1-methyl-2-[(2-methyl-2-propenyl)amino]-2-oxoethyl]carbamate

https://huagongshe.com/reaction/1491629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantTert-butoxycarbonylalanineHCID 85082—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant2-Methylallylamine hydrochlorideHCID 11953772—
SolventTetrahydrofuranHCID 8028—
Product(1,1-dimethylethyl) (S)-[1-methyl-2-[(2-methyl-2-propenyl)amino]-2-oxoethyl]carbamateHCID 5364295599.9%

Reaction Steps

To a cooled (0° C.) mixture of 18.9 parts of (S)-N-[(1,1-dimethylethoxy)carbonyl]alanine, 10.8 parts of 2-methyl-2-propen-1-amine monohydrochloride, 27.0 parts of 1-hydroxy-1H-benzotriazole hydrate and tetrahydrofuran, there were added 10.1 parts of N-methylmorpholine and, after 20 min, 20.6 parts of N,N-methanetetraylbis[cyclohexanamine] under a nitrogen atmosphere. The whole was kept at 0° C. for 1 hour and at room temperature for 12 hours. The solvent was evaporated and the residue was partitioned between dichloromethane and NaHCO3 (sat.). The organic layer was separated, washed with NaCl (sat.), dried, filtered and evaporated, yielding 24.2 parts (99.9%) of (1,1-dimethylethyl) (S)-[1-methyl-2-[(2-methyl-2-propenyl)amino]-2-oxoethyl]carbamate (interm. 63).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371079
Source datasetuspto-grants-1994_12
ORD IDord-2343737d8c60457ebe0660ca886c7918
Source noteuspto-grants-1994_12