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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233638Generated: October 31, 2026

6-chloro-N-(4-methoxyphenyl)pyridine-3-carboxamide → HCID 21914603, compound

https://huagongshe.com/reaction/2233638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-N-(4-methoxyphenyl)pyridine-3-carboxamideHCID 1483269—
ReactantN-cyclopropylmethyl-4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamideHCID 21914588—
ProductHCID 21914603HCID 21914603—

Reaction Steps

6-[5-Cyclopropylmethylcarbamoyl-2-methyl-phenyl]-N-(4-methoxyphenyl)-nicotinamide was prepared from 6-chloro-N-(4-methoxyphenyl)nicotinamide (Intermediate 2) and N-cyclopropylmethyl-4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide (Intermediate 10) using General Method B. LCMS: retention time 3.12 min, MH+ 416. NMR: δH [2H6]-DMSO 10.39,(1H, s), 9.21,(1H, d), 8.63,(1H, t), 8.41,(1H, dd), 7.96,(1H, s), 7.86,(1H, d), 7.79, (1H, d), 7.71,(2H, d), 7.44,(1H, d), 6.96,(2H, d), 3.76,(3H, s), 3.15,(2H, t), 2.41, (3H, s), 1.03,(1H, m), 0.43,(2H, m), 0.23,(2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709506B2
Source datasetuspto-grants-2010_05
ORD IDord-4fbc62559c6f4f01a18daaeaac91a763
Source noteuspto-grants-2010_05