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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649598Generated: October 30, 2026

Sodium hydride → HCID 13269938, compound

https://huagongshe.com/reaction/1649598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 19380105HCID 19380105—
ReactantHCID 86739134HCID 86739134—
SolventDimethylformamideHCID 6228—
ProductHCID 13269938HCID 1326993859.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 0.262 g of sodium hydride (55% dispersion in mineral oil) in 10 ml of N,N-dimethylformamide, 1.33 g (7 mmole) of 3-p-methoxyphenyl-5-pyrazolone was added portionwise with stirring under ice cooling. To the above mixture was added dropwise a solution of 3.05 g (5 mmole) of 1,4-dihydro-2,6-dimethyl-4-(2,3-dichlorophenyl)-3-methoxycarbonylpyridine-5-carboxylic acid 6-tosyloxyhexyl ester in 7 ml of N,N-dimethylformamide at 0° to 10° C. with stirring and then the mixture was heated at 80° C. for 3 hours. The resulting reaction mixture was poured into ice water, and the precipitate was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then evaporated in vacuo to obtain an oily residue. The residue was purified by silica gel column chromatography using a mixed solution of chloroform-methanol (the ratio by volume of 100:1) as an eluent, and the fractions containing desired compound were collected and evaporated in vacuo to dryness to give white crystalline residue. The residue was recrystallized from a mixed solution of ethyl acetate-normal hexane to give 1.87 g (yield 59.0%) of the 1,4-dihydro-2,6-dimethyl-4-(2,3-dichlorophenyl)-3-methoxycarbonylpyridine-5-carboxylic acid 6-(5-p-methoxyphenyl-3-pyrazolyloxy)hexyl ester as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04418197
Source datasetuspto-grants-1983_11
ORD IDord-baab7e440ecd4d0c9398b75a17310b17
Source noteuspto-grants-1983_11