Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186196Generated: October 31, 2026

3-Chloro-5-cyanopyridine-2-carboxylic acid → (R)-N-(3-(3-amino-6,6-difluoro-5-methyl-2,5,6,7-tetrahydro-1,4-oxazepin-5-yl)-4-fluorophenyl)-3-chloro-5-cyanopicolinamide formate

https://huagongshe.com/reaction/1186196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-5-cyanopyridine-2-carboxylic acidHCID 50853176—
Reactant(R)-5-(5-amino-2-fluorophenyl)-6,6-difluoro-5-methyl-2,5,6,7-tetrahydro-1,4-oxazepin-3-amineHCID 58562966—
Product(R)-N-(3-(3-amino-6,6-difluoro-5-methyl-2,5,6,7-tetrahydro-1,4-oxazepin-5-yl)-4-fluorophenyl)-3-chloro-5-cyanopicolinamide formateHCID 54577577—

Reaction Steps

The coupling of (R)-5-(5-amino-2-fluorophenyl)-6,6-difluoro-5-methyl-2,5,6,7-tetrahydro-1,4-oxazepin-3-amine (intermediate A10A) and 3-chloro-5-cyano-pyridine-2-carboxylic acid (prepared according to Hori, A. et al., Int. Patent Application Publ. No. WO2009151098) yielded the title compound as a pale yellow solid. MS (ISP): m/z=438.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673894B2
Source datasetuspto-grants-2014_03
ORD IDord-d65bbcf98163483e94a9f2822a579274
Source noteuspto-grants-2014_03