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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576898Generated: October 30, 2026

Dimethylformamide → HCID 89567430, compound

https://huagongshe.com/reaction/576898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 71512252HCID 71512252—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductAmmoniaHCID 2221%
ProductHCID 89567430HCID 8956743092%

Reaction Conditions

Temperature80 °C

Reaction Steps

DMF (2.99 mL) was slowly added to stirred sodium hydride (60% in oil; 51 mg, 1.28 mmol) and 2-chloro-N-methyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-4-amine (Intermediate I-15) (104 mg, 0.467 mmol) at room temperature. The mixture was warmed to 80° C. for 10 minutes, followed by addition of iodomethane (0.035 mL, 0.560 mmol). The mixture was stirred at 80° C. for 30 minutes, then cooled and diluted with saturated aqueous NaHCO3 (45 mL) and ethyl acetate (70 mL). After stirring for 10 minutes, the organic layer was separated and the aqueous layer was extracted with ethyl acetate (2×70 mL). The combined organic layers were evaporated onto silica gel. Gradient chromatography, eluting with 1-10% MeOH: 1% NH3 in CH2Cl2 over 10 column volume, gave 2-chloro-N,N-dimethyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-4-amine (102 mg, 0.431 mmol, 92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040540B2
Source datasetuspto-grants-2015_05
ORD IDord-7a9ca695c58743219b5da873c1fa863b
Source noteuspto-grants-2015_05