HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293927Generated: October 26, 2026
Sodium hydride → 2-Amino-6-chloro-9-[(diethylphosphonomethoxy)methoxymethyl]purine
https://huagongshe.com/reaction/2293927
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Amino-6-chloropurine | HCID 5360349 | — |
| Reactant | Chloromethoxy(diethylphosphonomethoxy)methane | HCID 14843539 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-6-chloro-9-[(diethylphosphonomethoxy)methoxymethyl]purine | HCID 14843540 | — |
Reaction Steps
To a suspension of 60% sodium hydride in mineral oil (1.4 g, 34.5 mmol) in DMF (100 mL) was added 2-amino-6-chloropurine (5.78 g, 34.2 mmol) and the mixture was stirred for 1 hr at 25° C. To the resulting yellow solution was added dropwise a solution of above chloromethoxy(diethylphosphonomethoxy)methane in DMF (20 mL) under nitrogen. After stirring 15 hr at 25° C., volatiles were removed in vacuo. The residual oil was suspended in ethyl acetate (100 mL), washed with water (30 mL), brine and dried (MgSO4). The solvent was removed under reduced pressure, and the residual oil was chromatographed on silica gel using CH2Cl2 /3% MeOH as eluent to give the title compound as a colorless oil: yield 3.0 g (23%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05688778 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-7ab93b45ff8c470a94f5908ff98ed6d3 |
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| Source note | uspto-grants-1997_11 |
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