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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472183Generated: October 29, 2026

1H-Pyrazol-3-amine, 5-methyl- → HCID 178419098, compound

https://huagongshe.com/reaction/472183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
Reactant4-Chloro-2-phenylpyrido[2,3-D]pyrimidineHCID 12203870—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178419098HCID 17841909850.7%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633210B2
Source datasetuspto-grants-2014_01
ORD IDord-6d8c1403c01c4ff7800b80ecc8c59cd3
Source noteuspto-grants-2014_01