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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985941Generated: October 30, 2026

Acetic Acid → HCID 13604742, compound

https://huagongshe.com/reaction/985941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylamineHCID 674—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 13604735HCID 13604735—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventHCID 86628739HCID 86628739—
ProductHCID 13604742HCID 13604742—

Reaction Steps

4.2 g (15 millimoles) of 6-[p-(3-formylpyrrol-1-yl)-phenyl]4, 5-dihydro-5-methylpyridazin-3-one (compound from Example 1A) in 30 ml of methanol were stirred with 3.36 g (30 millimoles) of 40% strength aqueous dimethylamine solution, 1.8 g (30 millimoles) of acetic acid and 0.75 g (12 millimoles) of sodium cyanoborohydride for 5 hours at room temperature (conversion monitored by thin layer chromatography using SiO2 and 5:2:2 ethyl acetate/acetic acid/water). 50 ml of H2O were added, the mixture was rendered alkaline with 2N NaOH and extracted with ethyl acetate, the organic phase was washed with water, dried with Na2SO4 and purified over a silica gel column using a 4:1 methylene chloride/methanol mixture, and the crystalline residue from the product-containing fractions was recrystallized from ethyl acetate/petroleum ether. 1.4 g of 6-[p-(3-dimethylaminomethylpyrrol-1-yl)-phenyl]-4, 5-dihydro-5-methylpyridazin-3-one of melting point 167°-168° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04710496
Source datasetuspto-grants-1987_12
ORD IDord-93bd8ca7de2f428e9564a42b092cc1f5
Source noteuspto-grants-1987_12