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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377045Generated: October 30, 2026

Acetic Acid → 3-Amino-9-bromobenzo[f]quinazolin-1(2H)-one

https://huagongshe.com/reaction/1377045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantN-(9-bromo-1,2-dihydro-1-oxobenzo[f]quinazolin-3-yl)pivalamideHCID 135838104—
SolventSodium HydroxideHCID 14798—
Product3-Amino-9-bromobenzo[f]quinazolin-1(2H)-oneHCID 135422913—

Reaction Conditions

Temperature75 °C

Reaction Steps

A solution of N-(9-bromo-1,2-dihydro-1-oxobenzo[f]quinazolin-3-yl)-pivalamide (0.15 g, 0.4 mmole) in 0.75N NaOH (7 ml) was stirred and heated to 75° C. under a nitrogen atmosphere for 10.5 hours. The solution was cooled and made slightly acidic with acetic acid to cause precipitation of the product. The precipitate was collected, washed successively with water, methanol and ether, and dried to give 3-amino-9-bromobenzo[f]quinazolin 1(2H)-one as an off-white solid. (0.115 g, 99%) 1H NMR (DMSO-d6, 200 MHz) δ: 6.64(br s, 2H, NH2); 7.31(d, J=8.8 Hz, 1H, Ar); 7.57(dd, J=8.5, 1.9 Hz, 1H, Ar); 7.83(d, J=8.6 Hz, 1H, Ar); 8.02(d, J=9.0 Hz, 1H, Ar); 9.83(s, H, Ar); 11.28(br s, 1H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663337
Source datasetuspto-grants-1997_09
ORD IDord-c186af750fe24c1891843b52082a66c0
Source noteuspto-grants-1997_09