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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206148Generated: November 1, 2026

Sodium hydride → 4-(1-(1-methoxybutan-2-yl)-4-oxo-4,5-dihydro-1H-pyrazolo[4,3-c]pyridin-3-yl)thiophene-2-carboxamide

https://huagongshe.com/reaction/2206148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Methoxybutan-2-yl 4-methylbenzene-1-sulfonateHCID 12700776—
Reactant4-(4-oxo-4,5-dihydro-1H-pyrazolo[4,3-c]pyridin-3-yl)thiophene-2-carboxamideHCID 137010709—
SolventDimethylformamideHCID 6228—
Product4-(1-(1-methoxybutan-2-yl)-4-oxo-4,5-dihydro-1H-pyrazolo[4,3-c]pyridin-3-yl)thiophene-2-carboxamideHCID 13701058532.8%

Reaction Steps

To a solution of 4-(4-oxo-4,5-dihydro-1H-pyrazolo[4,3-c]pyridin-3-yl)thiophene-2-carboxamide (50.0 mg) obtained in Step A of Example 141 in DMF (2 mL) was added sodium hydride (60% dispersion in mineral oil, 15.4 mg), and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added 1-methoxybutan-2-yl 4-methylbenzenesulfonate (99.0 mg) obtained in Step A-1 of Example 17, and the mixture was stirred overnight at room temperature. The reaction mixture was extracted with water and ethyl acetate, and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (basic silica gel, ethyl acetate/methanol) to give the title compound (21.8 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371320B2
Source datasetuspto-grants-2016_06
ORD IDord-52e7c3773fe941ac84f3815ff3b73c83
Source noteuspto-grants-2016_06