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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522609Generated: October 29, 2026

Sodium hydride → N-{1-[(6-methyl-2-pyridinyl)methyl]-1H-pyrazol-3-yl}acetamide

https://huagongshe.com/reaction/522609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-(Bromomethyl)-6-methylpyridineHCID 12543733—
ReactantHCID 178474341HCID 178474341—
SolventTetrahydrofuranHCID 8028—
ProductN-{1-[(6-methyl-2-pyridinyl)methyl]-1H-pyrazol-3-yl}acetamideHCID 8669160875%

Reaction Conditions

Temperature0 °C

Reaction Steps

Intermediate 1 (97 mg, 0.774 mmol) was dissolved in 8 mL of THF (anh), at 0° C. NaH (ALDRICH, 31 mg, 0.774 mmol) was added, and mixture of reaction was stirred at 0° C. for 30 minutes. A solution of Intermediate 11 (144 mg, 0.774 mmol) in 2 mL THF (anh) was added to the mixture. Reaction was heated at 75° C. overnight. Mixture of reaction was partitioned between distilled water, EtOAc (×3) and DCM. Organic layers were dried over MgSO4 (anh) and filtered. Solvent was evaporated under vacuum. Residue was purified by silica chromatography column using a linear gradient of DCM/MeOH as eluents to give the title compound (133 mg, 0.578 mmol, 75% yield). 1H NMR (300 MHz, DMSO-d6) ppm: 10.40 (br s, 1H), 7.72 (d, 1H), 7.60-7.66 (m, 1H), 7.17-7.16 (m, 1H), 6.74-6.77 (m, 1H), 6.49 (d, 1H), 5.24 (s, 2H), 2.44 (s, 3H), 1.95 (s, 3H). [ES+MS] m/z 231 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334265B2
Source datasetuspto-grants-2016_05
ORD IDord-dacca3c64840402392333b83763af68f
Source noteuspto-grants-2016_05