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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644209Generated: October 23, 2026

2-amino-N-(5-chloropyridin-2-yl)benzamide → 2-[4-(B enzyloxy)-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoylamino]-N-(5-chloropyridin-2-yl)benzamide

https://huagongshe.com/en/reaction/644209

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
Reactant4-Benzyloxy-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoic acidHCID 68535719—
Product2-[4-(B enzyloxy)-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoylamino]-N-(5-chloropyridin-2-yl)benzamideHCID 68532666—

Reaction Steps

Using methods substantially equivalent to those described in Example 1-F, 4-benzyloxy-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoic acid (529 mg, 1.27 mmol) and N-(5-chloropyridin-2-yl)-2-aminobenzamide (297 mg, 1.20 mmol) afforded, after purification by chromatography (SiO2: EtOAc in hexanes), 493 mg (63%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700628B2
Source datasetuspto-grants-2010_04
ORD IDord-b362c472deaa453eac5060bc7a1ee1e1
Source noteuspto-grants-2010_04