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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258650Generated: November 1, 2026

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

https://huagongshe.com/reaction/2258650

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 mole) 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, 1H, Ar); 11.28(br s, 1H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05661155
Source datasetuspto-grants-1997_08
ORD IDord-51236fbd295b400fb1ea83c20933084a
Source noteuspto-grants-1997_08