HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466684Generated: October 30, 2026
Sodium hydride → HCID 131717244, compound
https://huagongshe.com/reaction/466684
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazole | HCID 10053461 | — |
| Reactant | 6-Chloro-8-propyl-9H-purine | HCID 19012223 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131717244 | HCID 131717244 | — |
Reaction Steps
To a stirred suspension of NaH (0.016 g of a 60% dispersion in oil, 0.4 mmol) in dry dimethylformamide (1.5 ml) was added 6-Chloro-8-propylpurine (0.044 g, 0.25 mmol) at room temperature. After 20 minutes, the mixture was cooled to 0° C. and N-triphenylmethyl-5-(4'-bromomethylbiphen-2-yl)tetrazole (0.139 g, 0.25 mmol) was added. The resulting mixture was warmed to room temperature and then stirred at 40° C. for 3 hours. The reaction was cooled, and the content of the flask was poured into ice-water (50 ml) and extracted with ethyl acetate (3×15 ml). The combined organic phase was washed with brine and then dried over anhydrous Na2SO4. Removal of the solvent gave the crude product as a foam which was purified by flash-chromatography on silica-gel using ethyl acetate/hexane (1:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157026 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-3172d536e6bc4fafb15ea02aeadc4d87 |
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| Source note | uspto-grants-1992_10 |
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