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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113707Generated: October 30, 2026

Dimethylformamide → HCID 11551131, compound

https://huagongshe.com/reaction/2113707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 11543755HCID 11543755—
SolventWaterHCID 962—
ProductHCID 11551131HCID 1155113148%

Reaction Steps

5-[1-(4-Fluorophenyl)-1H-pyrazol-5-yl]-2-methoxyphenol (50.0 mg, 0.176 mmol), 5 mL of N,N-dimethylformamide and methyl iodide (16.4 uL, 0.264 mmol) were combined in a vial and stirred at room temperature overnight. An additional 0.5 mL of methyl iodide was added and stirring continued for 2 days at room temperature and then 10 mL of ethyl acetate and 10 mL of water were added. The organic layer was separated, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with a gradient of 10% ethyl acetate in hexanes to 50% ethyl acetate in hexanes over 20 minutes to give 5-(3,4-dimethoxyphenyl)-1-(4-fluorophenyl)-1H-pyrazole (25 mg, 48%) as a white solid. LC/MS (EI) tR 4.14, m/z 299.1 (M++1). 1H NMR (CDCl3 300 MHz) δ 3.7 (s, 3H); 3.9 (s, 3H); 6.5 (s, 1H); 6.7 (s, 1H); 7.0 (s, 2H); 7.1 (m, 2H); 7.3 (m, 2H); 7.7 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432266B2
Source datasetuspto-grants-2008_10
ORD IDord-e5e27386230747dd9fffea90194ab206
Source noteuspto-grants-2008_10