HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577788Generated: November 2, 2026
3-Amino-5-methylisoxazole → HCID 57486825, compound
https://huagongshe.com/reaction/577788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Amino-5-methylisoxazole | HCID 66172 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-((Cyclobutylmethyl)(ethyl)amino)quinoline-3-carbaldehyde | HCID 57444444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57486825 | HCID 57486825 | 43% |
Reaction Steps
5-Methyl-isoxazol-3-ylamine (0.098 g, 1 mmol) was added to a solution of 2-(cyclobutylmethyl-ethyl-amino)-quinoline-3-carbaldehyde (0.268 g, 1 mmol) in anhydrous methanol (5 mL) and acetic acid (0.15 mL) under nitrogen. After being stirred for 15 minutes at ambient temperature, sodium cyanoborohydride (0.19 g, 3 mmol) was added slowly, and the reaction mixture was stirred overnight. Afterwards, the solvent was evaporated in vacuo, and water (30 mL) and ethyl acetate (30 mL) were added to the residue. The organic layer was separated, washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by chromatography on silica gel, eluting with 1-5% methanol in dichloromethane, to afford the title compound (0.150 g), yield: 43%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040558B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-45eb516066b54c9791b39454285cebdb |
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| Source note | uspto-grants-2015_05 |
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