HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368088Generated: November 1, 2026
4-Methyl-1,2-oxazol-3-amine → HCID 58483990, compound
https://huagongshe.com/reaction/2368088
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methyl-1,2-oxazol-3-amine | HCID 13795047 | — |
| Reactant | HCID 67448291 | HCID 67448291 | — |
| Reactant | HCID 178419135 | HCID 178419135 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58483990 | HCID 58483990 | 68% |
Reaction Steps
To a solution of 1-({1-[6-(cyclopropylmethoxy)-1,3-benzoxazol-2-yl]piperidin-4-yl}oxy)propan-2-one (50 mg) and 4-methylisoxazol-3-amine (21.4 mg) in methanol (1 mL) and acetic acid (50 μL) was added decaborane (26.6 mg), and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate, washed with distilled water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography (NH, hexane/ethyl acetate). 1M Hydrochloric acid was added thereto, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (42.1 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703758B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-41bd571b42874f50ad12ae553add1a77 |
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| Source note | uspto-grants-2014_04 |
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