Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394153Generated: October 30, 2026

Tert-butyl 4-{[5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2-oxo-1,2-dihydro-1,6-naphthyridin-7-yl]amino}piperidine-1-carboxylate → 5-(2-Chlorophenyl)-1-(2,6-dichlorophenyl)-7-(piperidin-4-ylamino)-1,6-naphthyridin-2(1h)-one

https://huagongshe.com/reaction/394153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-{[5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2-oxo-1,2-dihydro-1,6-naphthyridin-7-yl]amino}piperidine-1-carboxylateHCID 22648019—
Reactant5-(2-Chlorophenyl)-1-(2,6-dichlorophenyl)-7-[(1-isopropylpiperidin-4-yl)amino]-1,6-naphthyridin-2(1h)-oneHCID 22648199—
Product5-(2-Chlorophenyl)-1-(2,6-dichlorophenyl)-7-(piperidin-4-ylamino)-1,6-naphthyridin-2(1h)-oneHCID 22648065—

Reaction Steps

The title compound was prepared from tert-butyl 4-{[5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2-oxo-1,2-dihydro-1,6-naphthyridin-7-yl]amino}piperidine-1-carboxylate by a procedure analogous to that described in EXAMPLE HHH2, Step C. Mass spectrum (ESI) 501 (M+1). Step C: 5-(2-Chlorophenyl)-1-(2,6-dichlorophenyl)-7-[(1-isopropylpiperidin-4-yl)amino]-1,6-naphthyridin-2(1H)-one

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809199B2
Source datasetuspto-grants-2004_10
ORD IDord-534338700a0c40288b6a1860fbb14a37
Source noteuspto-grants-2004_10