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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 176Generated: October 24, 2026

1-Isopropyl-3-methyl-1H-pyrazol-5-amine → Gsk-2256098

https://huagongshe.com/en/reaction/176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Isopropyl-3-methyl-1H-pyrazol-5-amineHCID 121018—
Reactant2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamideHCID 57516896—
ReagentCesium carbonateHCID 10796—
CatalystBinap, (A+-)-HCID 634876—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,4-DioxaneHCID 31275—
ProductGsk-2256098HCID 4621493045.14%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-(2,5-dichloropyridin-4-ylamino)-N-methoxybenzamide (200 mg, 0.64 mmol), 1-isopropyl-3-methyl-1H-pyrazol-5-amine (98 mg, 0.70 mmol) and cesium carbonate (626 mg, 1.92 mmol) were suspended in 1,4-dioxane (3 mL). Nitrogen was bubbled through mixture for 10 minutes. 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (39.9 mg, 0.06 mmol) and diacetoxypalladium (7.19 mg, 0.03 mmol) were added and tube was sealed. Mixture was stirred at reflux overnight. Reaction was allowed to cool to room temperature, filtered, washed with CH2Cl2/MeOH (9/1, 10 mL). Silica (63-200 µm) was added to the filtrate and mixture was concentrated to dryness. The crude product was purified by flash chromatography (dry loading) on silica gel eluting with 1 to 5% methanol in dichloromethane. The solvent was evaporated to dryness to afford 2-(5-chloro-2-(1-isopropyl-3-methyl-1H-pyrazol-5-ylamino)pyridin-4-ylamino)-N-methoxybenzamide (120 mg, 45.1 %) as a pale beige foam => _contaminated by a few BINAP or BINAP by-products_

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-327a3bfbd8b64cd3801bd5b8d317cb01
Source note750 AstraZeneca ELN dataset