Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035654Generated: November 1, 2026

cis-Tert-butyl 4-fluoro-5-(4-nitrophenylsulfonyloxy)azepane-1-carboxylate → (trans)-Tert-butyl 4-(2-(6-cyano-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-yloxy)-5-fluoroazepane-1-carboxylate

https://huagongshe.com/reaction/2035654

Reaction equation

Participants

RoleNameHCIDCharge
Reactantcis-Tert-butyl 4-fluoro-5-(4-nitrophenylsulfonyloxy)azepane-1-carboxylateHCID 131731015—
Reactant3-(8-Hydroxyquinolin-2-yl)[1,2,4]triazolo[4,3-a]pyridine-6-carbonitrileHCID 136400770—
Product(trans)-Tert-butyl 4-(2-(6-cyano-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-yloxy)-5-fluoroazepane-1-carboxylateHCID 131731024—

Reaction Steps

Prepared according to the method of Example 90, using cis-tert-butyl 4-fluoro-5-(4-nitrophenylsulfonyloxy)azepane-1-carboxylate in place of trans-tert-butyl 4-fluoro-5-(4-nitrophenylsulfonyloxy)azepane-1-carboxylate and 3-(8-hydroxyquinolin-2-yl)-[1,2,4]triazolo[4,3-a]pyridine-6-carbonitrile in place of 2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-6-fluoroquinolin-8-ol in Step C and running the reaction at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575145B2
Source datasetuspto-grants-2013_11
ORD IDord-0e24dbb3444940119800dc64594bcce4
Source noteuspto-grants-2013_11