Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 135838202 | HCID 135838202 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 135622210 | HCID 135622210 | 58.5% |
Reaction Steps
A solution of N-(1,2-dihydro-1-oxo-9-(trimethylsilylethynyl)benzo[f]quinazolin-3-yl)pivalamide (0.24 g, 0.61 mmol) and K2C03 (0.50 9'3.6 mmol) in methanol (-50 ml) was stirred at reflux for 2.5 hours. The solution was then diluted with water (-20 ml) acidified with acetic acid, and the resulting solid filtered and dried at 900 C under reduced pressure. The solid was resuspended in ethanol (- 20 ml), filtered, and dried to give 3-amino-9-ethynyl benzo[f]quinazolin- 1(2H)-one (0.084 g) as a tan solid. 1H NMR (DMSO-d, 200 MHz) δ: 4.26 (s, 1H, ethynyl CH), 6.63 (br s, 2H, NH2), 7.32 (d, J=9 Hz, 1H, Ar'), 7.47 (dd, J=8,2 Hz, 1H, Ar), 7.87 (d, J=8 Hz, IH, Ar), 8.02 (d, J =9 Hz, 1H, Ar), 9.78 (s, 1H, Ar), 11.34 (br s, 1H, NH). Mass spectrum (CI-CH4): 236 (M+1, 100%). Anal. Calculated for C1-4H9N3 0: (, 71.48; H, 3.86; N, 17.86. Found: C, 71.30; H, 3.92; N, 17.68.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090941 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-d9d6e6c33f4742bc98efafa61010792b |
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| Source note | uspto-grants-2000_07 |
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