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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403050Generated: October 30, 2026

Water → HCID 11247457, compound

https://huagongshe.com/reaction/403050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant[6-(Bromomethyl)pyridin-2-yl]methanolHCID 10878213—
ReactantN-cyclopropyl-3-[(4-hydroxybenzoyl)amino]-4-methylbenzamideHCID 66631169—
SolventAcetonitrileHCID 6342—
ProductHCID 11247457HCID 1124745758%

Reaction Steps

3-{[4-(hydroxy)benzoyl]amino}-N-cyclopropyl-4-methylbenzamide (100 mg, 0.323 mmol), [6-(bromomethyl)pyridin-2-yl]methanol (71 mg, 0.355 mmol) and potassium carbonate (49 mg, 0.355 mmol) were mixed in acetonitrile (3 mL) and the reaction was stirred at room temperature for 16 h. The reaction was then heated at 100° C. in the microwave for 10 mins. Water (10 mL) was added and the mixture was extracted with DCM (3×15 mL). The organic layers were combined and evaporated to give a white solid which was triturated with DCM to give the title compound as a white solid (80 mg, 58%); NMR Spectrum: (DMSOd6) 0.58 (m, 2H), 0.68 (m, 2H), 2.25 (s, 3H), 2.85 (m, 1H), 4.59 (s, 2H), 5.24 (s, 2H), 7.16 (d, 2H), 7.32 (d, 1H), 7.38 (d, 1H), 7.45 (d, 1H), 7.63 (m, 1H), 7.80 (m, 2H), 7.97 (d, 2H), 8.36 (d, 1H), 9.82 (s, 1H); Mass Spectrum: M+H+ 432.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742124B2
Source datasetuspto-grants-2014_06
ORD IDord-76c03a0446254cedacc7d4e51c93bd40
Source noteuspto-grants-2014_06