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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 6-Chloropurine | HCID 5359277 | — |
| Reactant | (S)-tert-Butyl 2-(((benzyloxy)carbonyl)amino)-3-hydroxypropanoate | HCID 11140975 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (s)-2-Benzyloxycarbonylamino-3-(6-chloro-purin-9-yl)-propionic acid tert-butyl ester | HCID 11384926 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747016B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-822b8fc58d8144c9805545109c5f6d27 |
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| Source note | uspto-grants-2004_06 |
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