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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416203Generated: November 1, 2026

N-(2-Aminoethyl)piperidine → HCID 10194112, compound

https://huagongshe.com/reaction/2416203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
ReactantHCID 10308794HCID 10308794—
ProductHCID 10194112HCID 10194112—

Reaction Conditions

Temperature128 °C

Reaction Steps

A mixture of 3-[2-(2-chloro-pyridin-4-yl)-thiazol-4-yl]-1H-quinolin-2-one (Example 85, 60 mg, 0.18 mmol) and 1-(2-aminoethyl)piperidine (Aldrich-Sigma Company, 2 mL) was heated at 128° C. for 48 h. The reaction was quenched by addition of 10 mL of H2O. The precipitates were collected by filtration and purified by Gilson preparative HPLC to provide the title compound as a yellow solid after lyophilization. MS m/z: 389.3 (M+1). HRMS m/z: 389.1398 (M+H+, C22H20N4OS Calc'd 389.1431).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822097B1
Source datasetuspto-grants-2004_11
ORD IDord-44c9470394f7459aa70d5e329cb5be7c
Source noteuspto-grants-2004_11