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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562702Generated: October 30, 2026

Ammonia → 2-Chloro-9-(tetrahydropyran-2-yl)adenine

https://huagongshe.com/reaction/562702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2,6-DichloropurineHCID 5324412—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-9-(tetrahydropyran-2-yl)adenineHCID 12777819—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2,6-dichloropurine (25 g) (available from, for example, Aldrich, UK) in dry ethyl acetate (200 ml) was added p-toluenesulfonic acid monohydrate (235 mg). The reaction was heated to 50° C. and 3,4-dihydro-2H-pyran (18.1 ml) was added in one go. The reaction was allowed to stir at 50° C. for 1 hour and the solvent was removed under reduced pressure. This afforded a yellow solid. A suspension of this solid (˜36 g) in 2.0M ammonia in isopropanol (460 ml) was heated under nitrogen at 60° C. for 4 hours with an attached condenser. The reaction was poured into water (50 ml) and left to cool overnight. The precipitate was filtered and dried on a rotary evaporator (60° C.) for 30 min. to afford the title compound as an off-white solid, 31 g (93%, 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067426B2
Source datasetuspto-grants-2011_11
ORD IDord-a4ab3448e7574de29cb818f628ef6fb5
Source noteuspto-grants-2011_11