HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-N-(3-bromophenyl)pyrido[2,3-d]pyrimidine-4,7-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | N-(3-bromophenyl)-7-fluoropyrido[2,3-d]pyrimidin-4-amine | HCID 5328268 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-N-(3-bromophenyl)pyrido[2,3-d]pyrimidine-4,7-diamine | HCID 5328267 | 90% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A solution of 4-(3-bromoanilino)-7-fluoropyrido[2,3-d]pyrimidine (0.20 g, 0.63 mmol) in EtOH (20 mL) is saturated with ammonia and warmed at 100° C. in a pressure vessel for 30 h. The solvent is removed under reduced pressure to give 7-amino-4-(3-bromoanilino)pyrido[2,3-d]pyrimidine (0.18 g, 90%). 1H NMR (DMSO) δ 9.97 (1H, brs), 8.59 (1H, s), 8.51 (1H, d, J=9.3 Hz), 8.11 (1H, sl brs), 7.77 (1H, brd, J=6.3 Hz), 7.44 (2H, brs), 7.37-7.30 (2H, m), 6.81 (1H, d, J=9.3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713484B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-a93115e1909d40c3965843845a5a529f |
| Source note | uspto-grants-2004_03 |