HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3,10-diamino-9-bromobenzo[f]quinazolin-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Amino-9-bromobenzo[f]quinazolin-1(2H)-one | HCID 135422913 | — |
| Reactant | N-(10-amino-9-bromo-1,2-dihydro-1-oxobenzo[f]quinazolin-3-yl)pivalamide | HCID 135838115 | — |
| Product | 3,10-diamino-9-bromobenzo[f]quinazolin-1(2H)-one | HCID 135838125 | — |
Reaction Steps
N-(10-Amino-9-bromo-1,2-dihydro-1-oxobenzo[f]quinazolin-3-yl)pivalamide (0.58 g, 1.5 mmoles) was reacted with aqueous sodium hydroxide as described for the analogous 9-bromo compound (example 2). The product was precipitated from the reaction mixture with acetic acid, filtered and washed with water to give 3,10-diamino-9-bromobenzo[f]quinazolin-1(2H)-one as a yellow solid. (0.36 g, 80%) 1H NMR (DMSO-d6, 200 MHz) δ: 6.49(br s, 2H, NH2); 6.69(br s, 1H, NH2); 7.09(d, J=8.4 Hz, 1H, Ar); 7.22(d, J=8.9 Hz, 1H, Ar); 7.56(d, J=8.4 Hz, 1H, Ar); 7.90(d, J=8.9 Hz, 1H, Ar); 11.47(br s, 1H, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663337 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-883248124c2a40c395682397c770bb90 |
| Source note | uspto-grants-1997_09 |