HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-3-phenoxy-2-propanol → 7-[3-(3-Phenoxy-2-hydroxypropylamino)-propyl]-theophylline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-3-phenoxy-2-propanol | HCID 94300 | — |
| Reactant | 7-(3-aminopropyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione | HCID 2965226 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-[3-(3-Phenoxy-2-hydroxypropylamino)-propyl]-theophylline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144340 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-efeded0832d9465981883351326e06bc |
| Source note | uspto-grants-1979_03 |