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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509101Generated: October 30, 2026

HCID 178452588, compound → HCID 178423072, compound

https://huagongshe.com/reaction/1509101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178452588HCID 178452588—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 178423072HCID 17842307263.4%

Reaction Steps

tert-butyl(1-(4-(4,4-dimethyl-8-phenyl-4,5-dihydro-2H-pyrazolo[3,4-f]quinolin-7-yl)phenyl)cyclobutyl)carbamate (8 mg, 0.015 mmol) was dissolved in TFA (0.5 mL) and stirred for 30 seconds. The solution was immediately concentrated to dryness under reduced pressure. The residue was dissolved in diethyl ether (˜1 mL) and concentrated to dryness under reduced pressure three times. The residue was then slurried in diethyl ether (1 mL) and after settling the supernatant solvent 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 (4 mg, 50% yield). 1H NMR (500 MHz, CH3OD) 8.18 (s, 1H), 7.63 (s, 1H), 7.47 (d, 2H), 7.41 (d, 2H), 7.19-7.33 (br m, 5H), 3.08 (s, 2H), 2.68-2.79 (br m, 2H), 2.51-2.64 (br m, 2H), 2.15-2.30 (br m, 1H), 1.87-2.01 (br m, 1H), 1.35 (s, 6H). LCMS (Method A): RT=3.03 min, M+H+=421.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-5583ca0c388446c38d21cb009d5c2e84
Source noteuspto-grants-2015_12