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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244891Generated: November 2, 2026

Triphenylphosphine → 2,6-dichloro-9-(tetrahydro-3-thienyl)-9H-purine

https://huagongshe.com/reaction/1244891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant2,6-DichloropurineHCID 5324412—
Reactant3-HydroxythiopheneHCID 10964421—
SolventTetrahydrofuranHCID 8028—
Product2,6-dichloro-9-(tetrahydro-3-thienyl)-9H-purineHCID 2192299124.8%

Reaction Steps

312 mg of 3-hydroxythiophene, 380 mg of 2,6-dichloropurine, 6 ml of tetrahydrofuran, 786 mg of triphenylphosphine (P(phenyl)3) are mixed together at ambient temperature then 0.47 ml of DEAD (diethyl-azodicarboxylate) is added over 10 minutes and agitation is carried out overnight at ambient temperature. Then 10 ml of NaH2PO4 in aqueous solution 1M is added, followed by extracting 3 times with 10 ml of methylene chloride, washing with 10 ml of water with 5 of an aqueous solution of sodium chloride, drying and evaporating to dryness. After purification on silica eluting with methylene chloride/ethyl acetate in a proportion of 75/25 then 90/10, impasting is carried out at ambient temperature in 5 ml of isopropyl ether, followed by separating, washing with 5 ml of isopropyl ether and drying at ambient temperature. In this way 137 mg of expected product is obtained in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122669B1
Source datasetuspto-grants-2006_10
ORD IDord-a6df9468db66439baf5795b9a1345237
Source noteuspto-grants-2006_10