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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654350Generated: November 1, 2026

Nitric Acid → HCID 135838168, compound

https://huagongshe.com/reaction/1654350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 23507948HCID 23507948—
ProductHCID 135838168HCID 135838168—

Reaction Steps

To a mixture of fuming nitric acid (7 ml) and sulphuric acid (6 ml) at 0° C. was added 1,3-diamino-8-bromo-5,6-dihydrobenzo[f]quinazoline (1.0 g, 3.4 mmoles) in a single portion. The reaction mixture was stirred at 0°-5° C. for 45 minutes, and then slowly poured onto ice (15 g). The resulting precipitate was filtered, washed with water (10 ml) and ether (10 ml), and resuspended in boiling 1N HCl (100 ml) for 1 hour. After cooling, the solid was filtered, triturated with hot ethanol, filtered again, washed with ethanol and ether, and dried to give 3-amino-8-bromo-9-nitrobenzo[f]quinazolin-1(2H)-one as a pale yellow solid. (0.59 g, 45%) 1H NMR(DMSO-d6, 80 MHz) δ: 7.62-7.71(d, J=7 Hz, 1H, Ar); 7.77(s, 3H, NH3+); 8.23-8.34(d, J=9 Hz, 1H, Ar); 8.59(s, 1H, Ar); 10.08(s, 1H, Ar). Anal. Calculated for C12H7BrN4O3.1 /2HNO3.H2O C, 37.47; H, 2.49; N, 16.39. Found C, 37.20; H, 2.24; N, 16.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405851
Source datasetuspto-grants-1995_04
ORD IDord-058eb39e17314250b068e87fa8bc5fce
Source noteuspto-grants-1995_04