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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489653Generated: October 31, 2026

HCID 22902333, compound → HCID 22902351, compound

https://huagongshe.com/reaction/1489653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22902333HCID 22902333—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 22902351HCID 2290235127%

Reaction Steps

4.9 g of 3-{3-[N-(2-(3,4-dimethoxyphenyl)-ethyl)-amino]-propyloxy}-2-benzyl-5-(3,4-dimethoxyphenyl)-pyrazole were dissolved in glacial acetic acid, 0.5 g of palladium on charcoal was added, and the reaction mixture was hydrogenated at 80 bar hydrogen pressure and at 80° C. for 24 hours. After removal of the catalyst by filtration, the reaction mixture was concentrated by evaporation and rendered alkaline (pH=10) with sodium hydroxide solution, and the product was extracted with ethyl acetate. The organic phase was separated, concentrated and purified by flash chromatography over silica gel. 1.1 g of 3-{3-[N-(2-(3,4-dimethoxyphenyl)-ethyl)-amino]-propyloxy}-5-(3,4-dimethoxyphenyl)-pyrazole were obtained. The IR spectrum of the base (as film) showed bands at 1511 cm-1, 1465 cm-1, 1262 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679699
Source datasetuspto-grants-1997_10
ORD IDord-293dbb2e8ce843228748189b981b4a9e
Source noteuspto-grants-1997_10