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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271676Generated: October 31, 2026

(6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone → {6-Bromo-4-[5-(2-(pyrrolidin-1-yl)ethyl)pyridin-3-ylamino]quinolin-3-yl}(cyclopropyl)methanone

https://huagongshe.com/reaction/2271676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanoneHCID 66715111—
Reactant5-(2-(Pyrrolidin-1-yl)ethyl)pyridin-3-amineHCID 66715736—
Product{6-Bromo-4-[5-(2-(pyrrolidin-1-yl)ethyl)pyridin-3-ylamino]quinolin-3-yl}(cyclopropyl)methanoneHCID 8669289645.3%

Reaction Steps

Following general procedure C, (6-bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone (262 mg, 0.845 mmol) was reacted with 5-[2-(pyrrolidin-1-yl)ethyl]pyridin-3-amine (161 mg, 0.845 mmol) to afford the desired product (178 mg, 45%) as a white solid: ESI MS m/z 465 [C24H25BrN4O+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-a22dcf56d76e44fdafd4987cf02fe534
Source noteuspto-grants-2015_09