HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923561Generated: November 1, 2026
4-Aminotetrahydropyran → 2-[(e)-2-(5-Methyl-3-phenyl-isoxazol-4-yl)-vinyl]-thiazole-5-carboxylic acid(tetra-hydro-pyran-4-yl)-amide
https://huagongshe.com/reaction/1923561
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminotetrahydropyran | HCID 419223 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 66643683 | HCID 66643683 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-[(e)-2-(5-Methyl-3-phenyl-isoxazol-4-yl)-vinyl]-thiazole-5-carboxylic acid(tetra-hydro-pyran-4-yl)-amide | HCID 49781807 | 59% |
Reaction Steps
To a stirred solution of 4-aminotetrahydropyran (123 mg, 1.22 mmol) in dioxane (3 mL) under argon and at room temperature was added trimethylaluminium (0.6 mL of a 2M solution in toluene, 1.2 mmol). After 1 h, a solution of 2-[(E)-2-(5-methyl-3-phenyl-isoxazol-4-yl)-vinyl]-thiazole-5-carboxylic acid ethyl ester (50 mg, 0.15 mmol) in dioxane (3 mL) was added and the reaction mixture heated at 90° C. for 3 h. The reaction mixture was then cooled, quenched with ice water and extracted with dichloromethane. The combined extracts were washed with Seignette's salt solution then dried, filtered, and concentrated. Purification by chromatography (silica, 0 to 2.5% methanol in dichloromethane) gave the title compound (34 mg, 59%) as a white solid. MS: m/e=396.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178522B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-e81960e92c454ae1a7622ce43806fe75 |
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| Source note | uspto-grants-2012_05 |
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