HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoaniline → HCID 18184379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | HCID 18184410 | HCID 18184410 | — |
| Reactant | 3-Bromoaniline--hydrogen chloride (1/1) | HCID 22736826 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 18184379 | HCID 18184379 | 104.5% |
Reaction Steps
A mixture of 4-methylthio-6H-imidazo[4,5-g]quinazoline (0.5 g, 1.6 mmol) [Leonard, N. J.; Morrice, A. G.; Sprecker, M. A.; J. Org. Chem., 1975, 40, 356-363], 3-bromoaniline (0.35 g, 2.0 mmol), and 3-bromoaniline hydrochloride (0.4 g, 1.9 mmol) in isopropanol (200 mL) is heated under reflux for 1 h to give a precipitate of 4-(3-bromoanilino)-6H-imidazo[4,5-g]quinazoline hydrochloride (0.63 g, 72%). 1H NMR (DMSO) δ9.93 (1H, brs), 9.01 (1H, s), 8.66 (2H, s), 8.39 (1H, s), 8.04 (2H, m), 7.39 (1H, t, J=7.9 Hz), 7.31 (1H, brd, J=8.0 Hz). ##STR22##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05679683 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-72e8c5b101194accb4dc22a56a80b69c |
| Source note | uspto-grants-1997_10 |