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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246029Generated: October 30, 2026

6-chloro-N-(cyclopropylmethyl)pyridine-3-carboxamide → HCID 21914628, compound

https://huagongshe.com/reaction/1246029

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-N-(cyclopropylmethyl)pyridine-3-carboxamideHCID 11275845—
Reactant4-Methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-N-(thiazol-2-yl)-benzamideHCID 21914517—
ProductHCID 21914628HCID 21914628—

Reaction Steps

N-Cyclopropylmethyl-6-[5-(thiazol-2-ylcarbamoyl)-2-methyl-phenyl]-nicotinamide was prepared from 6-chloro-N-cyclopropylmethylnicotinamide (Intermediate 1) and 4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-N-(thiazol-2-yl)-benzamide (Intermediate 11) using General Method B. LCMS: retention time 2.99 min, MH+ 393. NMR: δH [2H6]-DMSO 12.71,(1H, b), 9.13,(1H, s), 8.86,(1H, t), 8.34,(1H, d), 8.21,(1H, s), 8.07,(1H, d), 7.81,(1H, d), 7.57,(1H, d), 7.52,(1H, d), 7.29,(1H, d), 3.21,(2H, t), 2.45,(3H, s), 1.07,(1H, m), 0.47,(2H, m), 0.27,(2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125898B2
Source datasetuspto-grants-2006_10
ORD IDord-9ccc69db36cb4cb7b9d48b77e0bba97b
Source noteuspto-grants-2006_10