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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269361Generated: November 1, 2026

4-Methylmorpholine → HCID 86757664, compound

https://huagongshe.com/reaction/2269361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPentafluorophenolHCID 13041—
ReactantAcetic-formic anhydrideHCID 75269—
ReactantHCID 57069188HCID 57069188—
SolventPyridineHCID 1049—
ProductHCID 86757664HCID 8675766458%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2R,3S)-2-(3-phenyl-1-propyl)-3-(2-tetrahydropyranyloxyamino)hexanoic acid (0.93 g, 2.66 mmol) in pyridine (2 mL) at 0° C. is added formic acetic anhydride (0.4 mL). The resulting solution is stirred at 0° C. for 1 h, concentrated in vacuo, and diluted with 11 mL of EtOAc. To the solution of crude acid is added pentafluorophenol (0.51 g, 2.79 mmol), NMM (0.28 g, 2.79 mmol) and dicyclohexylcarbodiimide (0.58 g, 2.79 mmol). The resulting solution is stirred at 23° C. for 20 h and is filtered. The filtrate is washed with 1 N hydrochloric acid, 1 M aqueous sodium carbonate solution, and saturated aqueous sodium chloride solution. The organic layer is dried over magnesium sulfate, concentrated, and purified by silica gel chromatography (elution with 9:1 hexanes-EtOAc) to provide pentafluorophenyl (2R,3S)-2-(3-phenyl-1-propyl)-3-(formyl-2-tetrahydropyranyloxyamino)hexanoate as an oil (0.84 g, 58% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329400B1
Source datasetuspto-grants-2001_12
ORD IDord-47f432e8a8934f8b8d4a832498992289
Source noteuspto-grants-2001_12