HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797433Generated: November 2, 2026
Triphenylphosphine → HCID 86594457, compound
https://huagongshe.com/reaction/1797433
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-Amino-6-chloropurine | HCID 5360349 | — |
| Reactant | HCID 76386712 | HCID 76386712 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86594457 | HCID 86594457 | 65.6% |
Reaction Steps
To a suspension of 56 (120 mg, 0.32 mmol), triphenylphosphine (84.5 mg, 0.64 mmol), and 2-amino-6-chloropurine (108 mg, 0.64 mmol) in THF (10 mL) was added diethyl azodicarboxylate (111 mg, 0.64 mmol) at −20° C. The reaction mixture was stirred at −20° C. for 1 hour. It was poured into DCM (50 mL), washed with 0.5 N sodium hydroxide (3×10 mL), dried over sodium sulfate, and concentrated in vacuo. Purification via silica gel chromatography gave the title compound (0.11 g, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07034152B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-835f5e65a8e143eebb662a7328e810d4 |
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| Source note | uspto-grants-2006_04 |
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