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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375911Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 58709769, compound

https://huagongshe.com/reaction/2375911

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantN,N-DimethylethylenediamineHCID 66053—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 1280267HCID 1280267—
SolventWaterHCID 962—
ProductHCID 58709769HCID 58709769—

Reaction Steps

A stirred mixture of 3-[2-(3-nitrophenyl)-2-oxoethyl]-3H-quinazolin-4-one (2.00 g, 6.47 mmol), N,N-dimethyl-1,2-ethanediamine (2.28 g, 25.9 mmol), and p-toluenesulfonic acid (2.23 g, 12.9 mmol) in xylenes (150 mL) was refluxed for 48 h. After cooling to rt, water (20 mL) and sat. NaHCO3 (aq) (15 mL) were added. Layers were separated, and the aqueous phase was extracted with EtOAc (3×50 mL). The combined organic phases were dried over MgSO4, filtered, concentrated, and purified by silica gel chromatography (8% MeOH in CH2Cl2) to afford the desired product. 1H-NMR (CD3OD, 400 MHz): δ=2.15 (s, 6H), 2.54 (t, J=7.2 Hz, 2H), 4.22 (t, J=6.8 Hz, 2H), 7.15 (d, J=1.2 Hz, 1H), 7.74 (t, J=8.0 Hz, 1H), 7.89 (dt, J=2.4, 7.6 Hz, 1H), 7.90 (s, 1H), 8.24-8.26 (m, 1H), 8.30 (s, 1H). MS (ES+): m/z 261.24 [MH+]. HPLC: tR=0.49 and 0.71 min (ZQ2000, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465726B2
Source datasetuspto-grants-2008_12
ORD IDord-f9c38421d96e4d0cbc317795e8be666b
Source noteuspto-grants-2008_12