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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415608Generated: October 26, 2026

(2-Methylpyridin-4-yl)methanol → 2,6-Difluoro-3-[(2-methyl-4-pyridinyl)methoxy]benzenecarboxamide

https://huagongshe.com/reaction/415608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Methylpyridin-4-yl)methanolHCID 9942144—
Reactant2,6-Difluoro-3-hydroxybenzamideHCID 45120136—
Product2,6-Difluoro-3-[(2-methyl-4-pyridinyl)methoxy]benzenecarboxamideHCID 5940299034%

Reaction Steps

Synthesised from 2,6-difluoro-3-hydroxybenzenecarboxamide according to Method C, scheme 3. The required building block, 4-hydroxymethyl-2-methylpyridine, was synthesised according to the literature method, shown in Scheme 23 (Ragan, J. A., Jones, B. P., Meltz, C. N., Teixeira J. J. Jr.; Synthesis 2002, 483-486. Yield 34%, mp 185-186° C., HPLC-MS (method 1): m/z 279 [M+H]+, Rt=2.50 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088791B2
Source datasetuspto-grants-2012_01
ORD IDord-5ee878e59a1c44468ad7e53d661af8aa
Source noteuspto-grants-2012_01