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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352387Generated: October 30, 2026

Triphenylphosphine → (s)-2-Benzyloxycarbonylamino-3-(6-chloro-purin-9-yl)-propionic acid tert-butyl ester

https://huagongshe.com/reaction/352387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant6-ChloropurineHCID 5359277—
Reactant(S)-tert-Butyl 2-(((benzyloxy)carbonyl)amino)-3-hydroxypropanoateHCID 11140975—
SolventTetrahydrofuranHCID 8028—
Product(s)-2-Benzyloxycarbonylamino-3-(6-chloro-purin-9-yl)-propionic acid tert-butyl esterHCID 11384926—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 7.73 g (50 mmol) of 6-chloropurine in 350 ml of absolute THF were added 14.43 g (55 mmol) triphenylphosphine at −10 to 0° C. followed by 9.57 g (55 mmol) of diethyl azodicarboxylate and 14.8 g (50 mmol) of N-benzyloxycarbonyl-L-serine tert-butyl ester in 100 ml of absolute THF, and the mixture was stirred at 0° C. for 48 h. The solvent was evaporated, the residue was dissolved in EE/heptane (2:1), filtered and the solvent was removed in vacuo. The crude product was purified by flash chromatography on silica gel (EE/n-heptane (1:1) and DCM/EE (85:15)). Yield: 6.6 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747016B1
Source datasetuspto-grants-2004_06
ORD IDord-822b8fc58d8144c9805545109c5f6d27
Source noteuspto-grants-2004_06