Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741124Generated: October 27, 2026

4'-(5-Methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carboxylic acid → 1'-Ethyl-5-[4'-(5-methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carbonyl]-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine]

https://huagongshe.com/reaction/1741124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-(5-Methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carboxylic acidHCID 18797043—
Reactant1'-Ethyl-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine]HCID 21833744—
Product1'-Ethyl-5-[4'-(5-methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carbonyl]-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine]HCID 2183382231%

Reaction Steps

The title compound was prepared from 4'-(5-methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carboxylic acid (D11) and 1'-ethyl-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine] (D109) using a similar procedure as that outlined in Example 1, to afford the title compound as a yellow gum (31%). This was converted to its hydrochloride salt to yield an off white solid m.p. 245-249° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972951
Source datasetuspto-grants-1999_10
ORD IDord-1efe16ea59e2420ab79da6e6c297a9d5
Source noteuspto-grants-1999_10