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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872056Generated: October 31, 2026

Potassium Phosphate, Tribasic → 4-{[(1S,2S)-2-(5-methoxypyridin-2-yl)cyclopropyl]methoxy}-2-methyl-5-(1-methyl-1H-pyrazol-4-yl)pyrimidine

https://huagongshe.com/reaction/872056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant5-bromo-4-(((1S,2S)-2-(5-methoxypyridin-2-yl)cyclopropyl)methoxy)-2-methylpyrimidineHCID 71061385—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-{[(1S,2S)-2-(5-methoxypyridin-2-yl)cyclopropyl]methoxy}-2-methyl-5-(1-methyl-1H-pyrazol-4-yl)pyrimidineHCID 71061106—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromo-4-{[(1S,2S)-2-(5-methoxypyridin-2-yl)cyclopropyl]-methoxy}-2-methylpyrimidine (MM3) (400 mg, 1.1 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (420 mg, 2.0 mmol), tripotassium phosphate (600 mg, 2.8 mmol), S-Phos (46 mg, 0.1 mmol), and Pd(OAc)2 (12.6 mg, 0.6 mmol) in THF (4.8 mL) and water (0.8 mL) was heated at 100° C. for 1 hour. The reaction mixture was allowed to cool to room temperature, and then diluted with EtOAc (10 mL), washed with sodium bicarbonate (2 mL) and brine (2 mL), dried over MgSO4, filtered and concentrated. The resulting residue was purified by reverse phase chromatography (Waters Sunfire Prep C18 OBD, 5-45% acetonitrile in water with 0.1% TFA modifier) to afford the title compound as a colorless gum. 1H NMR (500 MHz, DMSO): δ 8.73 (s, 1 H), 8.14 (s, 1 H), 8.11 (s, 1 H), 7.97 (s, 1 H), 7.31-7.24 (m, 2 H), 4.54 (dd, J=11.2, 6.8 Hz, 1 H), 4.33 (dd, J=11.3, 7.7 Hz, 1 H), 3.82 (s, 3 H), 3.78 (s, 3 H), 2.50 (s, 3 H), 2.22 (dd, J=8.6, 4.7 Hz, 1 H), 1.79 (s, 1 H), 1.22-1.17 (m, 1 H), 1.10-1.05 (m, 1 H); HRMS m/z (M+H) 352.1761 found, 352.1768 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975261B2
Source datasetuspto-grants-2015_03
ORD IDord-7bca30b7b88e4861bfbce0dc95dc9fe2
Source noteuspto-grants-2015_03