HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342918Generated: October 30, 2026
Triphenylphosphine → HCID 54131397, compound
https://huagongshe.com/reaction/342918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | HCID 13964206 | HCID 13964206 | — |
| Reactant | HCID 178506933 | HCID 178506933 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54131397 | HCID 54131397 | — |
Reaction Steps
N6 -Benzoyl-9-(5-O-benzoyl-2-deoxy-β-D-threo-pentofuranosyl)adenine (7.0 g, 15.3 mmol), triphenylphosphine (6.0 g, 22.9 mmol), and LiN3 (2.8 g, 56.4 mmol) were dissolved in DMF (100 mL). To this stirring mixture was added diethylazodicarboxylate (3.6 mL, 22.9 mmol) in one portion, the reaction was stirred for 2.5 h at RT, and the reaction was quenched with H2O (10 mL). The solvents were removed in vacuo, the residual oil was redissolved in EtOAc (300 mL) and extracted with H2O (2×200 mL) and saturated. aq. NaCl (200 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residual oil was purified on SiO2 (2-5% MeOH/CH2Cl2) to afford 5'-O-Benzoyl-N2 -benzoyl-3'-azido-2',3'-dideoxyadenosine, 1a, as an amber foam, which was taken on directly to hydrogenation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859233 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-3ef0a14e99cc40ae920bf38dd7b4f8db |
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| Source note | uspto-grants-1999_01 |
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