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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509248Generated: November 1, 2026

HCID 86683635, compound → HCID 86683636, compound

https://huagongshe.com/reaction/1509248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86683635HCID 86683635—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 86683636HCID 8668363627%

Reaction Steps

Tert-butyl (1-(4-(8-phenyl-1-(trifluoromethyl)-4H-pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]oxazin-7-yl)phenyl)cyclobutyl)carbamate (7 mg, 0.012 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. This was repeated three times. The residue was then slurred in diethyl ether (2 ml) and after settling the supernatant solvent was removed by pipette. This was repeated three times. The residue was then slurred in n-hexane (2 ml) and after settling the supernatant solvent was 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 (1.5 mg, 26% yield). LCMS (Method D): RT=0.877 min, M+1=465. 1H-NMR (500 MHz, CD3OD) δ 8.02 (1H, s), 7.50 (2H, d), 7.43 (2H, d), 7.38-7.36 (3H, m), 7.25 (2H, m), 5.77 (2H, s), 2.75-2.69 (2H, m), 2.55-2.42 (2H, m), 2.29-2.17 (1H, m), 2.05-1.90 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-5f3e37a3bbd0442a8b14e396811e0813
Source noteuspto-grants-2015_12