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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2,6-Dichloropurine | HCID 5324412 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-9-(tetrahydropyran-2-yl)adenine | HCID 12777819 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08067426B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-a4ab3448e7574de29cb818f628ef6fb5 |
|---|
| Source note | uspto-grants-2011_11 |
|---|