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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035538Generated: October 31, 2026

Trimethyl orthoformate → 6-(1H-benzimidazol-1-yl)-4-[(3,5-difluorobenzyl)amino]pyridine-3-carboxyamide

https://huagongshe.com/reaction/2035538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant6-[(2-Aminophenyl)amino]-4-[(3,5-difluorobenzyl)amino]pyridine-3-carboxyamideHCID 131731001—
SolventMethanolHCID 887—
Product6-(1H-benzimidazol-1-yl)-4-[(3,5-difluorobenzyl)amino]pyridine-3-carboxyamideHCID 13173100294%

Reaction Steps

9 mg of 6-[(2-aminophenyl)amino]-4-[(3,5-difluorobenzyl)amino]pyridine-3-carboxyamide (the compound of step 1 of Example 365) was suspended in 0.2 ml of methanol, to which 0.2 mL of trimethyl orthoformate and a catalytic amount of p-toluenesulfonic acid monohydrate were added at room temperature, and stirred at the same temperature for 4 hours. The solvent was evaporated, saturated sodium bicarbonate was added to the residue, extracted with chloroform, the extract was washed with water, and dried on anhydrous sodium sulfate. The solvent was evaporated to obtain 9 mg (yield 94%) of the title compound as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575153B2
Source datasetuspto-grants-2013_11
ORD IDord-7ddf0498917045ffaba8f398893ef18f
Source noteuspto-grants-2013_11