HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069389Generated: October 29, 2026
Hydrochloric Acid → 2-Amino-7-benzyl-1H-purin-6(7H)-one
https://huagongshe.com/reaction/1069389
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 2-amino-9-[(2S,3R,4R,5R)-2,3,4-triacetyl-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one | HCID 137224663 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Amino-7-benzyl-1H-purin-6(7H)-one | HCID 135407703 | 80.5% |
Reaction Steps
Triacetylguanosine (0.756 g, 1.85 mmols) was suspended in 6 ml of acetonitrile, and 0.28 ml (1.25 equivalents) of benzyl bromide and 0.27 ml (1.25 equivalents) of benzyl chloride were added to the suspension. The mixture was reacted at 50° C. for 24 hours and at 60° for 23 hours. The temperature was returned to room temperature, and 1.58 ml (10.1 equivalents) of conc. hydrochloric acid were added thereto. The resulting mixture was reacted for 3 hours. After 40 minutes of the reaction, the solid was precipitated. Fifteen milliliters of methanol were added thereto, and the slurry was stirred for 1.5 hours, and then filtered. The crystals were washed twice with 5 ml of methanol, and dried at 50° C. under reduced pressure for 4 hours to give 0.468 g of 7-benzylguanine crystals in a yield of 80.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06252075B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-d3b8f9e20e3f4b79a4ed3634fd333d83 |
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| Source note | uspto-grants-2001_06 |
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