HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260143Generated: October 25, 2026
Ammonium Sulfate → 4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-one
https://huagongshe.com/reaction/260143
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Reactant | alpha-D-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-chlorobenzoate) | HCID 9845541 | — |
| Reactant | 4-Amino-2-phenyl-pteridine-7-one | HCID 54402511 | — |
| Catalyst | Silver perchlorate | HCID 24562 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexamethyldisilazane | HCID 13838 | — |
| Product | 4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-one | HCID 15403909 | — |
Reaction Steps
A mixture of 1.0 g (4.2 mmol) of 4-amino-2-phenyl-pteridine-7-one (3) and a few crystals of ammonium sulfate was heated in 100 mL of hexamethyldisilazane (HMDS) under reflux for 4 hours. After cooling the excess HMDS was distilled off in vacuum and the residue dissolved in 100 mL of dry toluene. To the mixture was added 2.17 g (4.6 mmol) of 2-deoxy-3,5-di-O-(4-chlorobenzoyl)-α-D-ribofuranosyl chloride (made as in Example 3, step (a) for the toluyl derivative) and 0.476 g (2.3 mmol) of silver perchlorate. The solution was then stirred under anhydrous conditions for 24 hours at room temperature and then diluted with 200 mL of CH2Cl2. The resulting AgCl precipitate was filtered off through silica and then the flitrate was treated with 100 mL of a saturated aqueous solution of sodium bicarbonate followed by 100 mL of a saturated aqueous solution of NaCl. The organic layer was dried over Na2SO4, filtered and then the flitrate evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05525711 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-709d959ee68d47eb90ce4ec250c5f310 |
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| Source note | uspto-grants-1996_06 |
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