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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341104Generated: October 30, 2026

Ammonium Chloride → HCID 68154122, compound

https://huagongshe.com/reaction/341104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69935372HCID 69935372—
SolventDichloromethaneHCID 6344—
ProductHCID 68154122HCID 68154122—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-(4-Aminobenzyl)-2-(2-methylphenyl)-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-one (Example 756, 35 mg, 0.092 mmol) and sodium bicarbonate (23 mg, 0.28 mmol, 3 equiv) were combined in dichloromethane (2 mL) and cooled to 0° C. The mixture was treated with methanesulfonyl chloride (0.071 mL, 0.92 mmol, 10 equiv), stirred for 4 hours and treated with ammonium chloride (0.2 mL, aqueous saturated). The mixture was diluted with dichloromethane (15 mL) and washed with brine (15 mL). The organic extract was dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by preparative reverse phase HPLC (eluting 80:20 to 5:95; water containing 0.1% trifluoroacetic acid:acetonitrile containing 0.1% trifluoroacetic acid), providing the title compound: 1H-NMR (400 MHz, CD3OD) δ 8.95 (1H, s), 8.34 (1H, d, J=7.8 Hz), 7.88 (1H, d, J=8.5 Hz), 7.70-7.66 (1H, m), 7.62-7.58 (1H, m), 7.47-7.38 (4H, m), 7.33-7.26 (4H, m), 5.76 (2H, s), 2.94 (3H, s), 2.27 (3H, s), ppm; low resolution mass spectrometry (ES+) m/z 458.9 [(M+H)+; calculated for C23H22N4O3S: 459.1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895580B2
Source datasetuspto-grants-2014_11
ORD IDord-ce7469cc967a4a3f92c981f0088c066e
Source noteuspto-grants-2014_11