HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388705Generated: October 30, 2026
4-Methylmorpholine → HCID 68644010, compound
https://huagongshe.com/reaction/2388705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | HCID 68644004 | HCID 68644004 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68644010 | HCID 68644010 | 23% |
Reaction Steps
To a solution of 5-(tert-butoxycarbonyl)-4-phenyl-4,5,6,7-tetrahydroisoxazolo-[4,5-c]pyridine-3-carboxylic acid (1.747 mmol, 1.0 eq.) in DMF (2 ml) was added BOP reagent (2.27 mmol, 1.3 eq.) and N-methyl morpholine (5.24 mmol, 3.0 eq.). The reaction mixture was stirred at room temperature for 15 min. A solution of piperidine (1.747 mmol, 1.0 eq.) in DMF (0.5 ml) was added to the reaction mixture and it was stirred for 12 h. The mixture was poured into water and resulting aqueous solution was extracted with ethyl acetate. The organic layer was successively washed with water and brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure to give the crude product which was purified by column chromatography (silica). Yield: 23%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268814B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-46a0e9ab2c6f4f09b0f0d4f82f815bf2 |
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| Source note | uspto-grants-2012_09 |
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