Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406356Generated: October 26, 2026

4-(N-Ethylaminocarbonyl)phenylboronic acid → 5-(4-Ethylaminocarbonyl-phenyl)-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]

https://huagongshe.com/reaction/2406356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(N-Ethylaminocarbonyl)phenylboronic acidHCID 3411307—
Reactant5-Chloro-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]HCID 86701200—
Product5-(4-Ethylaminocarbonyl-phenyl)-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]HCID 72194979—

Reaction Steps

The title compound is prepared from 5-chloro-1″-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1′-cyclobutane-3′,4″-piperidine] and 4-ethylaminocarbonyl-phenylboronic acid following a procedure analogous to that described for Example 1; the reaction is conducted in a microwave oven at 140° C. LC (method 3): tR=1.26 min; Mass spectrum (ESI+): m/z=478 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809361B2
Source datasetuspto-grants-2014_08
ORD IDord-2a1fc7c365b14d7a9e4c03fd5b333be1
Source noteuspto-grants-2014_08