Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296414Generated: October 30, 2026

Triphenylphosphine → (R)-1-(5-acetoxyhexyl)-8-bromo-7-(2-(N-tert-butoxycarbonylamino)ethyl)-3-methylxanthine

https://huagongshe.com/reaction/1296414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactanttert-butyl N-(3-hydroxypropyl)carbamateHCID 3838134—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(R)-1-(5-acetoxyhexyl)-8-bromo-3-methylxanthineHCID 69154488—
Solvent1,2-DichloroethaneHCID 11—
Product(R)-1-(5-acetoxyhexyl)-8-bromo-7-(2-(N-tert-butoxycarbonylamino)ethyl)-3-methylxanthineHCID 6915490087.1%

Reaction Steps

To a stirring suspension of (R)-1-(5-acetoxyhexyl)-8-bromo-3-methylxanthine (5.10 g, 13.2 mmol), triphenylphosphine (5.24 g, 20.0 mmol) and 3-(tert-butoxycarbonylamino)-1-propanol (3.2 g, 20.0 mmol) in anhydrous 1,2-dichloroethane (100 ml) at room temperature was added diethylazodicarboxylate (3.48 g, 20.0 mmol) dropwise. The mixture was stirred at room temperature overnight and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with ethyl acetate-hexane (1:1) to provide (R)-1-(5-acetoxyhexyl)-8-bromo-7-(2-(N-tert-butoxycarbonylamino)ethyl)-3-methylxanthine (6.10 g, 85% yield) as a beige oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247630B2
Source datasetuspto-grants-2007_07
ORD IDord-7a1c0ebfed1743d199f3d820bab72ee4
Source noteuspto-grants-2007_07