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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643862Generated: October 27, 2026

Pyridine → HCID 178489011, compound

https://huagongshe.com/reaction/643862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-4-methoxy-3-methylbenzamideHCID 59165435—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178489011HCID 178489011—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a suspension of 2-amino-4-methoxy-3-methyl benzamide in dry THF (60 ml) was added pyridine (2 eq) and the mixture was cooled to 5° C. 4-Methoxybenzoic acid chloride (1.25 eq) was added slowly and the mixture was stirred at room temperature overnight. The mixture was evaporated under reduced pressure and then suspended in water. The compound was left in the water for some hours, filtered and washed with cold water and diethyl ether and dried under vacuum. The residue was then added to a suspension of sodium carbonate (2.5 eq) in a 1:1 mixture of water and EtOH and the mixture was refluxed for two hours. The EtOH was removed under reduced pressure, a solution of 5% citric acid was added and the mixture was allowed to stay overnight. The title compound was isolated by filtration, then washed with water and diethyl ether and dried under vacuum. (5.5 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700552B2
Source datasetuspto-grants-2010_04
ORD IDord-e222cfa629204d4f841fa099f4b6f96f
Source noteuspto-grants-2010_04