HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11831Generated: October 25, 2026
1H-Pyrazol-3-amine, 5-methyl- → HCID 178419098, compound
https://huagongshe.com/reaction/11831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-Pyrazol-3-amine, 5-methyl- | HCID 93146 | — |
| Reactant | 4-Chloro-2-phenylpyrido[2,3-D]pyrimidine | HCID 12203870 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178419098 | HCID 178419098 | 50.7% |
Reaction Steps
To a solution of 4-chloro-2-phenyl-pyrido[2,3-d]pyrimidine (J. Pharm. Belg., 29, 1974, 145–148) (109 mg, 0.45 mmol) in THF (15 mL) was added 3-amino-5-methyl pyrazole (48 mg, 0.5 mmol) and the resulting mixture heated at 65° C. overnight. The mixture was cooled to room temperature and the resulting suspension was filtered and washed with Et2O. The solid was dissolved in a mixture EtOH:water and the pH adjusted to pH 7. The aqueous was extracted twice with ethyl acetate and the combined organic layers were dried (MgSO4), filtered, and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, DCM-MeOH gradient) to afford IV-31 as an off-white solid (69 mg, 50%): mp 234° C.; 1H NMR (DMSO) δ 2.14 (3H, s), 5.99 (1H, s), 7.20–7.40 (3H, m), 7.40–7.50 (3H, m), 8.60 (1H, d), 8.79 (1H, d), 12.82 (1H, br s); IR (solid) 2957, 2921, 2857, 1644, 1560, 1459, 1427; MS 303.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07098330B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-74bd5f909fdd45cab060be5e2f1707cd |
|---|
| Source note | uspto-grants-2006_08 |
|---|