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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400773Generated: October 30, 2026

5-Methyl-6-(2-methylpiperidin-1-yl)nicotinic acid → HCID 178423042, compound

https://huagongshe.com/reaction/400773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methyl-6-(2-methylpiperidin-1-yl)nicotinic acidHCID 58443364—
ReactantN'-hydroxy-3H-benzimidazole-5-carboximidamideHCID 178513241—
ProductHCID 178423042HCID 178423042—

Reaction Steps

Title compound was prepared following general procedure 1 starting from Intermediate 13 (120 mg; 0.51 mmol) and Intermediate 1 (90 mg; 0.51 mmol). Reaction mixture was filtered over a SPE-NH2 column, washed with THF followed by evaporation of the solvent under reduced pressure. Purification by silica column chromatography (EtOAc/c-Hex, 30/70 to 100/0) afforded the title compound as a brown powder. 1H NMR (DMSO, d6): δ 12.78 (s, 1H), 8.39-8.37 (m, 2H), 8.31 (s, 1H), 8.24 (dd, J=8.8, 2.2 Hz, 1H), 7.95-7.92 (m, 1H), 7.78-7.75 (m, 1H), 7.32 (d, J=8.8 Hz, 1H), 4.23-4.22 (m, 1H), 3.38-3.35 (m, 2H), 1.82-1.57 (m, 6H), 1.17 (d, 6.6 Hz, 3H). HPLC (Method A) Rt 2.71 min (Purity: 86.6%). LC/MS (method B): 358.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741923B2
Source datasetuspto-grants-2014_06
ORD IDord-63f608bafa0345158501ae4fdf20caaf
Source noteuspto-grants-2014_06