HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805257Generated: November 3, 2026
4-Methylmorpholine → HCID 67151588, compound
https://huagongshe.com/reaction/1805257
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 5-Ethoxypyrazine-2-carboxylic acid | HCID 57475692 | — |
| Reactant | HCID 67151626 | HCID 67151626 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67151588 | HCID 67151588 | 96.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354441B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-dd4a540497094cb4961db9b088068d6a |
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| Source note | uspto-grants-2013_01 |
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