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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198911Generated: November 2, 2026

Ammonia → 2,6-Diamino-9-(2-hydroxyethoxymethyl)purine

https://huagongshe.com/reaction/2198911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-Chloro-9-(2-hydroxyethoxymethyl)adenineHCID 12899586—
Product2,6-Diamino-9-(2-hydroxyethoxymethyl)purineHCID 9458812%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-chloro-9-(2-hydroxyethoxymethyl)adenine (4.4 g) and liquid ammonia (40 ml) was heated at 120° C. in a bomb for 19 hours. The reaction mixture was removed from the bomb and excess ammonia removed in vacuo. The residue was partitioned between ether and water and the aqueous layer washed twice more with ether and once with chloroform. The aqueous solution was then treated with an excess of a strongly basic ion exchange resin to convert the ammonium chloride to ammonia and evaporated to dryness in vacuo. The residue was dissolved in a minimal amount of ethanol, Florisil (Registered Trade Mark) (10g) added, and the mixture evaporated in dryess. The residue was transferred to a prepared column of Florisil in chloroform and eluted with 5% methanol/95% chloroform (v/v). Fractions (30 ml) were collected and examined by TLC (silica gel plates developed in 10% methanol/90% chloroform) for the presence of product. The first 40 fractions contained starting material but no product and were discarded. Succeeding fractions which were found to contain the desired product were combined and evaporated to dryness. The residue was recrystallized from ethanol (with activated charcoal treatment) and from n-propanol to give 2-amino-9-(2-hydroxyethoxymethyl)adenine (0.5 g, 12% of theoretical), m.p. 183°-184° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04360522
Source datasetuspto-grants-1982_11
ORD IDord-8c32d43ad07c4cd0b46e1b89fc18ae07
Source noteuspto-grants-1982_11