HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279210Generated: October 30, 2026
2-Naphthalenesulfonyl chloride → HCID 69557677, compound
https://huagongshe.com/reaction/1279210
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 69558158 | HCID 69558158 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69557677 | HCID 69557677 | 49.7% |
Reaction Steps
A solution of (3aS,4S,6R,6aR)-6-{2-(aminomethyl)-6-[(2,2-diphenylethyl)amino]-9H-purin-9-yl}-N-ethyl-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxamide (Preparation 10) (140 mg, 0.25 mmol) and triethylamine (0.05 ml, 0.36 mmol) in anhydrous dichloromethane (1 ml) was treated with a solution of 2-naphthalenesulfonyl chloride (63 mg, 0.28 mmol) in anhydrous dichloromethane (1 ml). The mixture was stirred at room temperature for 18 hours during which time the solvent was allowed to evaporate off freely. The residue was dissolved in ethanol (1 ml), treated with hydrochloric acid (1M, 1 ml) and heated at 60° C. for 15 hours. The solvent was removed under reduced pressure and the residue was azeotroped with ethanol (×2). The residue was then purified by column chromatography on silica gel eluting with a gradient system of dichloromethane:methanol (95:5 by volume) gradually changing to dichloromethane:methanol (90:10 by volume) to give a solid which was triturated with diethyl ether, diluted with pentane, filtered and dried to afford the title compound as a solid (88 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448236B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-21053c2fb46a4335831211573c3817d2 |
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| Source note | uspto-grants-2002_09 |
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