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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008Generated: October 23, 2026

Hydrochloric Acid → 4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridine

https://huagongshe.com/en/reaction/1008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
ReactantMagnesiumHCID 5462224—
Reactant4-(4-Oxocyclohexylamino)-3-methoxy-2-methylpyridineHCID 19693951—
SolventDiethyl EtherHCID 3283—
Product4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridineHCID 67671140—

Reaction Steps

A Grignard solution is prepared from 1.2 g of magnesium and 12.9 g of 90% strength 4-tert-butylbenzyl bromide in 100 ml of abs. ether. 2.9 g of 4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine in 50 ml of absolute THF are added dropwise to this solution. After 17 hours at room temperature it is acidified with 25 ml of 2N HCl, the mixture is extracted several times with ethyl acetate and the combined ethyl acetate phases are washed with sodium hydrogen carbonate solution. Purification is carried out by column chromatography on silica gel using ethyl acetate to which increasing amounts of methanol are added.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723450
Source datasetuspto-grants-1998_03
ORD IDord-77b579259b0e47c2ac2dc691717deb93
Source noteuspto-grants-1998_03