Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805257Generated: November 3, 2026

4-Methylmorpholine → HCID 67151588, compound

https://huagongshe.com/reaction/1805257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant5-Ethoxypyrazine-2-carboxylic acidHCID 57475692—
ReactantHCID 67151626HCID 67151626—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67151588HCID 6715158896.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of (4S,5S)-4-[2-(4-amino-phenyl)-ethyl]-2,2,5-trimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (120 mg) and 5-ethoxypyrazine-2-carboxylic acid (72.4 mg) in THF (3 ml) were added N-methylmorpholine (158 μl) and TBTU (230 mg). The reaction mixture was capped and shaken at 50° C. overnight. The crude reaction mixture was concentrated in vacuo and the residue was purified by flash chromatography (silica gel, gradient: 0% to 70% EtOAc in hexane) to afford (4S,5S)-4-(2-{4-[(5-ethoxy-pyrazine-2-carbonyl)-amino]-phenyl}-ethyl)-2,2,5-trimethyl-oxazolidine-3-carboxylic acid tert-butyl ester as a white solid (167 mg, 96%). MS (ISP): 507.3 ([M+Na]+), 502.3 ([M+NH4]+), 485.3 ([M+H]+), 429.3 ([M-C4H8]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354441B2
Source datasetuspto-grants-2013_01
ORD IDord-dd4a540497094cb4961db9b088068d6a
Source noteuspto-grants-2013_01