HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970271Generated: November 2, 2026
HCID 67246795, compound → HCID 59272361, compound
https://huagongshe.com/reaction/1970271
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 67246795 | HCID 67246795 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methyl butyrate | HCID 12180 | — |
| Product | HCID 59272361 | HCID 59272361 | 49.6% |
Reaction Steps
To a solution of 7-(3-methoxy-3-methylbut-1-ynyl)-3-(pyridin-3-yl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazol]-2′-amine (110 mg, 0.258 mmol) in 1:1 methanol ethyl acetate (10 mL) was added Pd/C (5%) (274 mg, 2.58 mmol). The resulting slurry was maintained under 1 atm of hydrogen gas for 4 hours at which point another loading of Pd/C (5%) (274 mg, 2.58 mmol) was added and the reaction was maintained under 1 atm of hydrogen gas for an additional 3 hours. The reaction was filtered through a pad of celite, washing well with methanol and ethyl acetate. The derived mixture was filtered through a 0.1 micron frit and concentrated to provide 7-(3-methoxy-3-methylbutyl)-3-(3-pyridinyl)spiro[chromeno[2,3-b]pyridine-5,4′-[1,3]oxazol]-2′-amine (55 mg, 0.128 mmol, 49.5% yield) as a light yellow solid. MS m/z=431.2 [M+H]+. Calc'd for C25H27N4O3: 431.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426447B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-d29fe7c57fed46b6b08ffcf4353a5d6b |
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| Source note | uspto-grants-2013_04 |
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