HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265966Generated: November 1, 2026
4-Methylmorpholine → HCID 72335659, compound
https://huagongshe.com/reaction/2265966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate | HCID 23149411 | — |
| Reactant | HCID 68781732 | HCID 68781732 | — |
| Reactant | 3-Ethynyl-5-fluoro-4-methansulfonylaminobenzylamine hydrochloride | HCID 86625519 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 72335659 | HCID 72335659 | 79.5% |
Reaction Steps
To a suspension of 3-ethynyl-5-fluoro-4-methansulfonylaminobenzylamine hydrochloride (67 mg, 0.24 mmol) m THF (2 mL) was added N-methylmorpholine (40 μL, 0.36 mmol). After stirring for 5 minutes, 3-(6-methoxy-4-trifluoromethylpyridin-3-yl)acrylic acid (50 mg, 0.20 mmol) dissolved in THF (3 mL) and 4-(4,6-dimethoxy[1,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (DMTMM, 67 mg, 0.24 mmol) were added. The mixture was stirred at room temperature overnight and concentrated under reduced pressure. The residue was diluted with EtOAc and water. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by recrystallization from EtOAc/hexane to give N-(3-ethynyl-5-fluoro-4-methanesulfonylaminobenzyl)-3-(6-methoxy-4-trifluoromethylpyridin-3-yl)acrylamide (75 mg, 66.2%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858621B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-99f265c09ff94ab7b472f2dc2a7c9ac2 |
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| Source note | uspto-grants-2010_12 |
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