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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014957Generated: October 31, 2026

Diisopropylethylamine → HCID 178463182, compound

https://huagongshe.com/reaction/1014957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 270265—
ReactantHCID 178463186HCID 178463186—
SolventIsopropanolHCID 3776—
ProductHCID 178463182HCID 17846318291.8%

Reaction Steps

(2R,3R,4R,5R)-2-{6-[(trans-4-Aminocyclohexyl)amino]-2-chloro-9H-purin-9-yl}-5-(2-ethyl-2H-tetrazol-5-yl)tetrahydrofuran-3,4-diyl diacetate (Intermediate 4) (7.9 g) was dissolved in isopropanol (200 ml) and stirred at room temperature under nitrogen. N,N-diisopropylethylamine (10 ml) was added followed by 2,6-dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (3.92 g). The mixture was stirred at 60° C. under nitrogen for 18 h. The reaction mixture was allowed to cool to room temperature and evaporated down in vacuo. The residue was partitioned between ethyl acetate and water. The organic phase was separated and the aqueous extracted twice with ethyl acetate. The organic phases were combined, dried (MgSO4), and evaporated down in vacuo to give the title compound (10.35 g). Used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985740B2
Source datasetuspto-grants-2011_07
ORD IDord-e601ac6747994d42b2b1e22fabd4c5c1
Source noteuspto-grants-2011_07