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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271542Generated: November 3, 2026

1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-amine → 1-(6-bromo-4-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)amino)quinolin-3-yl)ethanone

https://huagongshe.com/reaction/2271542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-amineHCID 53302346—
Reactant1-(6-Bromo-4-chloroquinolin-3-YL)ethanoneHCID 66715483—
Product1-(6-bromo-4-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)amino)quinolin-3-yl)ethanoneHCID 6671608452.1%

Reaction Steps

Following general procedure C, 1-(6-bromo-4-chloroquinolin-3-yl)ethanone (285 mg, 1.0 mmol) was reacted with 1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-amine (0.30 g, 1.66 mmol) to afford the desired product (223 mg, 52%) as a light yellow solid. ESI MS m/z 428 [C20H22BrN5O+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-f797d76638a8462c8b44b96ab6989276
Source noteuspto-grants-2015_09