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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271629Generated: November 1, 2026

Tert-butyl 1-(5-aminopyridin-2-yl)pyrrolidin-3-ylcarbamate → Tert-butyl 1-(5-(6-bromo-3-(cyclopropanecarbonyl)quinolin-4-ylamino)pyridin-2-yl)pyrrolidin-3-ylcarbamate

https://huagongshe.com/reaction/2271629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 1-(5-aminopyridin-2-yl)pyrrolidin-3-ylcarbamateHCID 53470939—
Reactant(6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanoneHCID 66715111—
ProductTert-butyl 1-(5-(6-bromo-3-(cyclopropanecarbonyl)quinolin-4-ylamino)pyridin-2-yl)pyrrolidin-3-ylcarbamateHCID 8669288388.3%

Reaction Steps

Following General procedure C, (6-bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone (311 mg, 1 mmol) was reacted with tert-butyl 1-(5-aminopyridin-2-yl)pyrrolidin-3-ylcarbamate (417 mg, 1.5 mmol) to afford the desired product (488 mg, 88%) as a yellow solid: ESI MS m/z 552 [C27H30BrN5O3+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-8062ecdc1cef4dccbdf6a916d1f4ce77
Source noteuspto-grants-2015_09