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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578413Generated: October 30, 2026

4-Phenylpiperidine → HCID 21559958, compound

https://huagongshe.com/reaction/1578413

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenylpiperidineHCID 69873—
Reactant4-(4-Chlorophenyl)piperidineHCID 1203613—
ReactantPyridine, 1,2,3,6-tetrahydro-4-[4-(trifluoromethyl)phenyl]-HCID 12440708—
ReactantHCID 21559977HCID 21559977—
ProductHCID 21559958HCID 21559958—
ProductHCID 21559976HCID 21559976—
ProductHCID 54020821HCID 54020821—

Reaction Steps

In the manner described in Example 1, reaction of 5-propionyl-6-methyl-6,7-dihydro-7-(2-bromoethyl)-5H-1,3-dioxolo[4,5-f]indole with 4-phenylpiperidine, 4-(p-chlorophenyl)piperidine, or 1,2,3,6-tetrahydro-4-(α,α,α-trifluoro-p-tolyl)pyridine provides the corresponding 5-propionyl-6-methyl-6,7-dihydro-7-[2-(4-phenylpiperidino) ethyl]-5H-1,3-dioxolo[4,5-f]indole, 5-propionyl-6-methyl-6,7-dihydro-7-{2-[4(p-chlorophenyl)piperidino]ethyl}-5H-1,3-dioxolo-[4,5-f]-indole, and 5-propionyl-6-methyl-6,7-dihydro-7-{2-[3,6-dihydro-(α,α,α-trifluoro-p-tolyl)-1(2H)-pyridyl]ethyl}-5H-1,3-dioxolo[4,5-f]indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03936464
Source datasetuspto-grants-1976_02
ORD IDord-04261106b6794e838c10000248fcb3a0
Source noteuspto-grants-1976_02