HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273262Generated: October 29, 2026
4-Isoxazolemethanamine → HCID 22274015, compound
https://huagongshe.com/reaction/273262
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Isoxazolemethanamine | HCID 10486803 | — |
| Reactant | HCID 86596640 | HCID 86596640 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22274015 | HCID 22274015 | 10% |
Reaction Steps
A solution of the methanesulfonic acid 5-{4-[5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenyl}-pyridin-2-ylmethyl ester 106 (220 mg, 0.5 mmol) in DMF (4.0 mL) was treated with C-isoxazol-4-yl-methylamine (68 mg, 0.5 mmol, 1.0 equiv) at room temperature, and the resulting reaction mixture was warmed to 60° C. and stirred for 6 hours. When TLC and MS showed the reaction to be complete, the reaction mixture was concentrated in vacuo, and the residue was directly purified by column chromatography (0-5% MeOH/CH2Cl2 gradient elution) to afford the desired N-{3-[3-Fluoro-4-(6-{[(isoxazol-4-ylmethyl)-amino]-methyl}-pyridin-3-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide 4252 (22 mg, 10%) as off-white solids. LCMS (EI): 440 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456206B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-67529b8e1e384cccb24717eac535e1e6 |
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| Source note | uspto-grants-2008_11 |
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