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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543488Generated: November 1, 2026

HCID 12915870, compound → HCID 12875762, compound

https://huagongshe.com/reaction/543488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12915870HCID 12915870—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 12875762HCID 1287576295%

Reaction Steps

2.31 g of 1-[2-hydroxy-2-(3,4-dibenzyloxyphenyl)-1-ethyl]-4-(2-keto-1-benzimidazolinyl)-piperidine hydrochloride is dissolved in 250 ml of methanol. 0.3 g of palladium carbon (10%) is added thereto, and the mixture is vigorously shaked in a hydrogen stream under atmospheric pressure. After discontinuation of the absorption of hydrogen, the catalyst is filtered off, and the mother liquor is concentrated. To the residual syrup is added ethyl acetate, and the mixture is well stirred. The mixture is filtered to obtain powdered product, and the product is washed with ethyl acetate and dried to obtain 1.52 g of 1-[2-hydroxy-2- (3,4-dihydroxyphenyl)-1-ethyl]-4-(2-keto-1-benzimidazolinyl)-piperidine hydrochloride as amorphous powder. When subjected to thin layer chromatography using a lower layer of a mixture of chloroform/methanol/acetic acid/water (10/10/1/10), this product provides single spot at Rf =0.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04446141
Source datasetuspto-grants-1984_05
ORD IDord-756b32047b07466583cbcd3b6ea236f4
Source noteuspto-grants-1984_05