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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433554Generated: October 29, 2026

tert-Butyl 4-(bromomethyl)piperidine-1-carboxylate → Tert-butyl 4-(((4-(3-chloro-4-((cyclopropylamino)carbonyl)aminophenoxy)-6-cyano-7-quinolyl)oxy)methyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/1433554

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(bromomethyl)piperidine-1-carboxylateHCID 15512811—
Reactantn-(4-(6-Cyano-7-hydroxy-4-quinolyl)oxy-2-chlorophenyl)-n'-cyclopropylureaHCID 135829385—
ProductTert-butyl 4-(((4-(3-chloro-4-((cyclopropylamino)carbonyl)aminophenoxy)-6-cyano-7-quinolyl)oxy)methyl)-1-piperidinecarboxylateHCID 2293657614.6%

Reaction Steps

The title compound (275.8 mg, 0.466 mmol, 14.6%) was obtained as white crystals from an N-(4-(6-cyano-7-hydroxy-4-quinolyl)oxy-2-chlorophenyl)-N′-cyclopropylurea crude product (1.00 g, 3.20 mmol) and tert-butyl 4-(bromomethyl)-1-piperidinecarboxylate, by the same procedure as in Example 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-ac51ab8085f243598f53dc3244f48a7e
Source noteuspto-grants-2009_11