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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970271Generated: November 2, 2026

HCID 67246795, compound → HCID 59272361, compound

https://huagongshe.com/reaction/1970271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67246795HCID 67246795—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethyl butyrateHCID 12180—
ProductHCID 59272361HCID 5927236149.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426447B2
Source datasetuspto-grants-2013_04
ORD IDord-d29fe7c57fed46b6b08ffcf4353a5d6b
Source noteuspto-grants-2013_04