HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543488Generated: November 1, 2026
HCID 12915870, compound → HCID 12875762, compound
https://huagongshe.com/reaction/543488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 12915870 | HCID 12915870 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12875762 | HCID 12875762 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04446141 |
|---|
| Source dataset | uspto-grants-1984_05 |
|---|
| ORD ID | ord-756b32047b07466583cbcd3b6ea236f4 |
|---|
| Source note | uspto-grants-1984_05 |
|---|