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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495434Generated: October 31, 2026

Pyridine → HCID 22326675, compound

https://huagongshe.com/reaction/495434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Amino-6-methoxybenzaldehydeHCID 22326715—
SolventTolueneHCID 1140—
ProductHCID 22326675HCID 2232667585.4%

Reaction Steps

To a stirred solution of 2-amino-6-methoxybenzaldehyde [K. Tsuda et al., Chem. Pharm. Bull. 1962, 10, 856] (1.3 g, 8.6 mmol), pyridine (0.81 g, 10.3 mmol) and toluene (60 mL) was added acetic anhydride (0.97 g, 9.5 mmol). The resulting mixture was heated at reflux for 18 h, cooled, then partitioned between saturated aqueous NaHCO3 (100 mL) and ether (50 mL). The organic phase was dried (Na2SO4) and evaporated in vacuo to give a solid which was purified by chromatography on silica with 0-50% ether in hexane gradient elution to give a colourless solid (1.28 g). The latter was dissolved in 2 M methanolic ammonia (100 mL) and the solution heated at reflux for 3 h, cooled, then evaporated in vacuo. Chromatography of the residue on silica with 0-100% ether in dichloromethane gradient elution gave the title compound (0.92 g, 62%) as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939871B2
Source datasetuspto-grants-2005_09
ORD IDord-4d77b185639146b6ba1250fa2431021a
Source noteuspto-grants-2005_09