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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986364Generated: October 29, 2026

Morpholine → 4-[(2RS, 3S)-3-(tertbutoxycarbonyl)amino-4-cyclohexyl-2-hydroxybutyryl]morpholine

https://huagongshe.com/reaction/986364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(2RS, 3S)-3-tert-butoxycarbonylamino-4-cyclohexyl-2-hydroxybutyric acidHCID 59490980—
SolventEthyl AcetateHCID 8857—
Product4-[(2RS, 3S)-3-(tertbutoxycarbonyl)amino-4-cyclohexyl-2-hydroxybutyryl]morpholineHCID 86741927—

Reaction Steps

To a solution of 200 mg of (2RS, 3S)-3-tertbutoxycarbonylamino-4-cyclohexyl-2-hydroxybutyric acid which was prepared in Reference Example 4, 0.06 ml of morpholine and 13 mg of 1-hydroxybenzotriazole in 6 ml of ethyl acetate was added 150 mg of dicyclohexylcarbodiimide with stirring under ice-cooling, and the mixture was stirred for 16 hours at room temperature. The reaction mixture was cooled, and filtered to remove insoluble materials. The filtrate was washed successively with an aqueous citric acid solution, a 5% aqueous sodium bicarbonate solution and a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and evaporated under reduced pressure to obtain 296 mg of 4-[(2RS, 3S)-3-(tertbutoxycarbonyl)amino-4-cyclohexyl-2-hydroxybutyryl]morpholine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04711958
Source datasetuspto-grants-1987_12
ORD IDord-128c961c545a4341a85802fcb4e6bc9b
Source noteuspto-grants-1987_12