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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271607Generated: October 31, 2026

Tert-butyl 1-(5-aminopyridin-2-yl)piperidin-3-ylcarbamate → Tert-butyl 1-(5-(6-bromo-3-propionylquinolin-4-ylamino)pyridin-2-yl)piperidin-3-ylcarbamate

https://huagongshe.com/reaction/2271607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 1-(5-aminopyridin-2-yl)piperidin-3-ylcarbamateHCID 66715840—
Reactant1-(6-Bromo-4-chloroquinolin-3-yl)propan-1-oneHCID 86692845—
ProductTert-butyl 1-(5-(6-bromo-3-propionylquinolin-4-ylamino)pyridin-2-yl)piperidin-3-ylcarbamateHCID 6671628121.4%

Reaction Steps

Following general procedure B, 1-(6-bromo-4-chloroquinolin-3-yl)propan-1-one (235 mg, 0.792 mmol) was reacted with tert-butyl 1-(5-aminopyridin-2-yl)piperidin-3-ylcarbamate (348 mg, 1.19 mmol) to afford the desired product (94 mg, 21%) as an orange solid: ESI MS m/z 554, [C27H32BrN5O3+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-a1ae990e5b004bb49b541f8955e2f352
Source noteuspto-grants-2015_09