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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654344Generated: November 1, 2026

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

https://huagongshe.com/reaction/1654344

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405851
Source datasetuspto-grants-1995_04
ORD IDord-d25ca860649f4be6bd084e1150376ac2
Source noteuspto-grants-1995_04