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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651414Generated: October 23, 2026

Benzaldehyde → 3-Chloro-2-ethyl-4-(2-phenyl-1,3-dioxan-5-ylamino)-pyridine

https://huagongshe.com/en/reaction/651414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSerinolHCID 68294—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant5-Chloro-6-ethyl-4-(1,3-dihydroxy-2-propylamino)-pyridineHCID 15346451—
Reactant3,4-Dichloro-2-ethylpyridineHCID 21708425—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-Chloro-2-ethyl-4-(2-phenyl-1,3-dioxan-5-ylamino)-pyridineHCID 9880046—

Reaction Steps

2.3 g (10 mmol) of 5-chloro-6-ethyl-4-(1,3-dihydroxy-2-propylamino)-pyridine (prepared analogously to Example A from 2-amino-1,3-propanediol and 3,4-dichloro-2-ethyl-pyridine) and 5.0 g of benzaldehyde were heated with 2.1 g of p-toluenesulfonic acid hydrate in 40 ml of toluene, using a water separator, until the evolution of water had ended. Working up and purification were carried out analogously to Example A. the chromatography over silica gel (ethyl acetate) gave initially 0.6 g of trans isomer (18.8% of theory), melting point: 139-140° C., and then 2.4 g of cis isomer (75.2% of theory), melting point 119-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281221B1
Source datasetuspto-grants-2001_08
ORD IDord-986edda2c1a54907ba8a915b5cd211e7
Source noteuspto-grants-2001_08