Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644239Generated: October 28, 2026

2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamide → HCID 68571380, compound

https://huagongshe.com/reaction/644239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamideHCID 21906418—
ReactantHCID 68536834HCID 68536834—
ReactantHCID 68570681HCID 68570681—
ProductHCID 68571380HCID 68571380103.8%

Reaction Steps

Using methods substantially equivalent to those described in Example 60-I and J, 5-chloro-N-(5-chloropyridin-2-yl)-2-[4-isopropyl-2-(piperidin-3-ylmethoxy)-benzoylamino]benzamide trifluoroacetate (150 mg, 0.20 mmol, 6%) was prepared from 2-(N-tert-butoxycarbonylpiperidin-3-yl)-4-isopropylmethoxybenzoic acid and N-(5-chloropyridin-2-yl)-2-amino-5-chlorobenzamide. This product was subjected to reverse phase HPLC to obtain 60 mg of the title compound as the hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700628B2
Source datasetuspto-grants-2010_04
ORD IDord-52e81bba604a4298b6cef5c2063fdded
Source noteuspto-grants-2010_04