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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242948Generated: October 31, 2026

4-Methylmorpholine → HCID 68157891, compound

https://huagongshe.com/reaction/242948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 62415716HCID 62415716—
SolventDichloromethaneHCID 6344—
ProductHCID 68157891HCID 6815789169.4%

Reaction Steps

A mixture of N2-cyclobutyl-4-fluorobenzene-1,2-diamine (0.63 g, 3.5 mmol), (S)-2-tertbutoxycarbonylaminopropionic acid (0.73 g, 3.9 mmol), HOAt (0.53 g, 3.9 mmol), 4-methylmorpholine (0.85 mL, 7.7 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.75 g, 3.9 mmol) in DCM (12 mL) was stirred at RT for 18 h. The reaction mixture was partitioned between DCM and a saturated aqueous solution of NaHCO3. The organic fraction was washed with brine, dried (MgSO4), concentrated in vacuo and the resulting residue purified by column chromatography (Si—PCC, gradient 0-30% EtOAc in cyclohexane) to afford [(S)-1-(2-cyclobutylamino-4-fluorophenylcarbamoyl)ethyl]carbamic acid tert-butyl ester (853 mg, 69%). LCMS (Method J): RT 3.54 min [M+H]+ 352.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-c6edad281db94e0d808ac230db7304ae
Source noteuspto-grants-2014_02