HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807494Generated: October 30, 2026
Isopropylamine → 6-(3-Butyl-5-methyl-isoxazol-4-ylmethoxy)-N-isopropyl-nicotinamide
https://huagongshe.com/reaction/1807494
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 6-(3-Butyl-5-methyl-isoxazol-4-ylmethoxy)-nicotinic acid methyl ester | HCID 66599158 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Diisopropyl Ether | HCID 7914 | — |
| Product | 6-(3-Butyl-5-methyl-isoxazol-4-ylmethoxy)-N-isopropyl-nicotinamide | HCID 49804756 | 30.6% |
Reaction Steps
Trimethylaluminium (3 mL of a 2 M solution in toluene, 6 mmol) was added dropwise to a stirred solution of isopropylamine (355 mg, 6.0 mmol) in dioxane (4 mL) at room temperature and under argon. After 1 h, a solution of 6-(3-butyl-5-methyl-isoxazol-4-ylmethoxy)-nicotinic acid methyl ester (537 mg, 1.5 mmol) in dioxane (4 mL) was added and the reaction mixture warmed to 90° C. After 2 h the reaction mixture was cooled and poured onto ice/water. The resultant mixture was extracted with ethyl acetate then the combined extracts were washed with Seignette salt solution. The organic phase was dried, filtered and evaporated then purified by chromatography (silica, 0 to 60% ethyl acetate in heptane) then trituration with diisopropyl ether to give the title compound (76 mg, 15%) as a white solid. MS: m/e=332.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357703B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-32b91403c47441a58bc7cde75647b43a |
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| Source note | uspto-grants-2013_01 |
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