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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2,6-Dichloropurine | HCID 5324412 | — |
| Reactant | 3-Hydroxythiophene | HCID 10964421 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-dichloro-9-(tetrahydro-3-thienyl)-9H-purine | HCID 21922991 | 24.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07122669B1 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-a6df9468db66439baf5795b9a1345237 |
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| Source note | uspto-grants-2006_10 |
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