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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509193Generated: November 2, 2026

HCID 86683598, compound → HCID 53262241, compound

https://huagongshe.com/reaction/1509193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86683598HCID 86683598—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 53262241HCID 5326224131.3%

Reaction Steps

Tert-butyl (1-(4-(8-phenyl-1-propyl-4H-pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]oxazin-7-yl)phenyl)cyclobutyl)carbamate (39 mg, 0.073 mmol) was dissolved in TFA (1 ml) and stirred for 30 seconds. The solution was immediately concentrated to dryness under reduced pressure. The residue was dissolved in diethyl ether (˜2 ml) and concentrated to dryness under reduced pressure three times. The residue was then slurred in diethyl ether (2 ml) and after settling the supernatant solvent removed by pipette. This was repeated three times. The residue was then slurred in n-hexane (2 ml) and after settling the supernatant solvent removed by pipette. This was repeated three times. The remaining solvent was removed under reduced pressure and the residue was dried to give the desired product as an off-white solid (10 mg, 30% yield). LCMS (Method A): RT=3.85 min, M+1=439. 1H-NMR (500 MHz, CD3OD) δ 8.09 (1H, s), 7.50 (2H, d), 7.43 (2H, d), 7.37-7.34 (3H, m), 7.31-7.27 (2H, m), 5.66 (2H, s), 3.2 (2H, t), 2.83-2.71 (2H, m), 2.64-2.54 (2H, m), 2.32-2.19 (1H, m), 2.02-1.90 (1H, m+2H, t), 1.16-1.09 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-9f672eafb27a443a8c44d6965495d82e
Source noteuspto-grants-2015_12