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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-(9-bromo-1,2-dihydro-1-oxobenzo[f]quinazolin-3-yl)pivalamide | HCID 135838104 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-Amino-9-bromobenzo[f]quinazolin-1(2H)-one | HCID 135422913 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05661155 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-51236fbd295b400fb1ea83c20933084a |
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| Source note | uspto-grants-1997_08 |
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