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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509270Generated: October 30, 2026

HCID 86683649, compound → HCID 53262565, compound

https://huagongshe.com/reaction/1509270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86683649HCID 86683649—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 53262565HCID 5326256592%

Reaction Steps

Tert-butyl (1-(4-(1-isopropyl-8-phenyl-4H-pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]oxazin-7-yl)phenyl)cyclobutyl)carbamate (24 mg, 0.045 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-hexanes (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 dried to give the desired product as an off-white solid (18 mg, 92% yield). LCMS (Method D) RT=0.815 min, M+1=438. 1H-NMR (500 MHz, CD3OD) δ 8.18 (1H, s), 7.52-7.47 (2H, m), 7.45-7.41 (2H, d), 7.38-7.34 (3H, m), 7.31-7.26 (2H, m), 5.64 (2H, s), 2.82-2.72 (2H, m), 2.63-2.54 (2H, m), 2.30-2.19 (1H, m), 2.02-1.92 (1H, m), 1.51 (6H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-c978f03efbcb475c83a071affe17abd0
Source noteuspto-grants-2015_12