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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889348Generated: October 29, 2026

6-chloro-N-(4-methoxyphenyl)nicotinamide → HCID 21914603, compound

https://huagongshe.com/reaction/889348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-N-(4-methoxyphenyl)nicotinamideHCID 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 numberUS08252818B2
Source datasetuspto-grants-2012_08
ORD IDord-79f876d6ad104f219d58a7a3734fdfce
Source noteuspto-grants-2012_08