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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355406Generated: November 2, 2026

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

https://huagongshe.com/reaction/1355406

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 numberUS06586429B2
Source datasetuspto-grants-2003_07
ORD IDord-6fea98f11c444c23bfb1f67c4d0f61e9
Source noteuspto-grants-2003_07