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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256292Generated: October 26, 2026

Phenylboronic Acid → HCID 67064830, compound

https://huagongshe.com/reaction/1256292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Chloro-2-methylpyrazolo(1,5-a)pyrimidin-5-amineHCID 44251307—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 67064830HCID 6706483018%

Reaction Conditions

Temperature100 °C

Reaction Steps

7-Chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-amine (1J, 10 g, 55 mmol), phenylboronic acid (7.3 g, 60 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]-dichloropalladium(II) (1.0 g, 1.4 mmol) were mixed in dioxane (120 ml) and saturated NaHCO3 (60 ml). The mixture was then heated at 100° C. for 4 hours. After cooling to room temperature, Brine was added and the mixture was extracted with EtOAc five times. Combined organics were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The crude product was purified by column chromatography (SiO2) to give 2-methyl-7-phenylpyrazolo[1,5-c]pyrimidin-5-amine (10A, 2.2 g, 18%) as a solid. 1H NMR (400 MHz, DMSO-d6) δ=7.95-7.85 (m, 2 H), 7.62-7.50 (m, 3 H), 6.70 (s, 2 H), 6.22 (s, 1 H), 5.81 (s, 1 H), 2.24 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461163B2
Source datasetuspto-grants-2013_06
ORD IDord-8d04edf5a904431389804c48195a1d99
Source noteuspto-grants-2013_06