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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394150Generated: October 29, 2026

1-Tert-butyl-4-[(trimethylstannyl)methylene]piperidine → 7-[(1-Tert-butylpiperidin-4-ylidene)methyl]-5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-1,6-naphthyridin-2(1h)-one

https://huagongshe.com/reaction/394150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butyl-4-[(trimethylstannyl)methylene]piperidineHCID 22647936—
ReactantHCID 22647982HCID 22647982—
Product7-[(1-Tert-butylpiperidin-4-ylidene)methyl]-5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-1,6-naphthyridin-2(1h)-oneHCID 22647891—

Reaction Steps

The title compound was prepared from 7-bromo-5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-1,6-naphthyridin-2(1H)-one (COMPOUND HHH2) and 1-tert-butyl-4-[(trimethylstannyl)methylene]piperidine (INTERMEDIATE ABA3)by a procedure analogous to that described in EXAMPLE HHH1, Step A. Mass spectrum (ESI) 554 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809199B2
Source datasetuspto-grants-2004_10
ORD IDord-24bdabdfad0b48fea3ab42ba12d36e74
Source noteuspto-grants-2004_10