Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051592Generated: October 31, 2026

4-Methylmorpholine → HCID 178454166, compound

https://huagongshe.com/reaction/2051592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 54234050HCID 54234050—
ReactantHCID 178454358HCID 178454358—
SolventEthyl AcetateHCID 8857—
ProductHCID 178454166HCID 178454166—

Reaction Steps

A mixture of NαNim -bis BOC-(S)-histidine ethyl acetate solvate (0.96 g, 2.50 mmol), 4 methyl-morpholine (0.28 mL, 2.50 mmol) and isobutyl chloroformate (0.33 mL, 2.50 mmol) in ethyl acetate (35 mL) is stirred in an ice bath under N2 for 15 minutes. A solution of (S)-2-amino-1-ethylthio-4-methyl pentane (0.40 g, 2.50 mmol) in ethyl acetate (2 mL) is then added and the reaction stirred at room temperature for 18 hours. After washing with 10% citric acid, brine, saturated NaHCO3 solution and brine, the ethyl acetate extract is dried (Na2SO4), filtered and concentrated under reduced pressure. The residue is flash chromatographed over silica gel. Elution with a mixture of 2% methanol- 98% chloroform affords pure BOC-protected histidineamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05019647
Source datasetuspto-grants-1991_05
ORD IDord-ae6280ed18d54d29b9533559572c5f97
Source noteuspto-grants-1991_05