HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83305Generated: October 29, 2026
Cyclopropylamine → N-Cyclopropyl-6-{[3-(4-fluoro-phenyl)-5-methyl-isoxazol-4-ylmethyl]-amino}-nicotinamide
https://huagongshe.com/reaction/83305
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 6-{[3-(4-Fluoro-phenyl)-5-methyl-isoxazol-4-ylmethyl]-amino}-nicotinic acid methyl ester | HCID 68443392 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-Cyclopropyl-6-{[3-(4-fluoro-phenyl)-5-methyl-isoxazol-4-ylmethyl]-amino}-nicotinamide | HCID 42629450 | 61.4% |
Reaction Steps
A solution of trimethylaluminium (2 M in toluene, 410 μL, 0.8 mmol) was added dropwise (exothermic) to a solution of cyclopropylamine (47 mg, 58 μL, 0.8 mmol) in dioxane (5 mL) and the resulting mixture was stirred at room temperature for 1 h. Then a solution of 6-{[3-(4-fluoro-phenyl)-5-methyl-isoxazol-4-ylmethyl]-amino}-nicotinic acid methyl ester (70 mg, 0.2 mmol) in dioxane (2.5 mL) was added. The resulting mixture was then heated at 85-95° C. for 5 h and then cooled to room temperature and then poured into a sodium potassium tartrate solution and extracted with ethyl acetate which was then washed with brine, dried over sodium sulfate and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 0:100) afforded the title compound (45 mg, 60%) which was obtained as an off white foam. MS: m/e=367.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846719B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-3bd623ca78944411876711ca0cbf7c63 |
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| Source note | uspto-grants-2014_09 |
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