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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010966Generated: October 30, 2026

2-Pentanol → 2-[(1-Methylbutyl)oxy]-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine

https://huagongshe.com/reaction/1010966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PentanolHCID 22386—
Reactant2-Chloro-9-(tetrahydropyran-2-yl)adenineHCID 12777819—
ReactantSodium t-butoxideHCID 23676156—
Product2-[(1-Methylbutyl)oxy]-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amineHCID 57699589—

Reaction Steps

To 2-pentanol (3.65 mL) was added sodium tert-butoxide (760 mg) in portions over 5 mins. The mixture was stirred at room temperature until homogeneous. 2-Chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine (500 mg) was added and the reaction was heated at 50° C. overnight, then for a further 72 h. The reaction mixture was cooled and quenched with water (10 mL) and was extracted with EtOAc (3×25 mL). The organics were combined, washed with brine (30 mL), dried over MgSO4, filtered and concentrated in vacuo to give crude title compound as a viscous yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977344B2
Source datasetuspto-grants-2011_07
ORD IDord-cf585b508a12478bb8564f00fc3c87d9
Source noteuspto-grants-2011_07