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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614326Generated: October 25, 2026

1-Chloro-3-phenoxy-2-propanol → 7-[3-(3-Phenoxy-2-hydroxypropylamino)-propyl]-theophylline

https://huagongshe.com/reaction/614326

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-3-phenoxy-2-propanolHCID 94300—
Reactant7-(3-aminopropyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dioneHCID 2965226—
SolventEthanolHCID 702—
Product7-[3-(3-Phenoxy-2-hydroxypropylamino)-propyl]-theophyllineHCID 21329278—

Reaction Steps

A mixture of 75 g of 7-(3-aminopropyl)-theophylline and 27.4 g of 1-chloro-3-phenoxy-2-propanol is heated for 8 hours at 130° to 140° C. After the melt has been cooled to 70°-90° C., ethanol is added to it, followed by brief boiling under reflux. After standing overnight, the untreated and precipitated aminopropyl theophylline hydrochloride is filtered off under suction, the filtrate is acidified with alcoholic hydrochloric acid, heavily concentrated and acetone added until crystallisation begins. The reaction product then separates and is recrystallised from methanol. Yield 30.2 g. Melting point of the hydrochloride: 183°-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04144340
Source datasetuspto-grants-1979_03
ORD IDord-efeded0832d9465981883351326e06bc
Source noteuspto-grants-1979_03