HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 482455Erstellt: 26. Oktober 2026
Dimethylformamide → 1-Adamantanecarbonyl chloride
https://huagongshe.com/reaction/482455
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Adefovir | HCID 60172 | — |
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | Adamantoyl oxymethyl chloride | HCID 14699931 | — |
| Produkt | 1-Adamantanecarbonyl chloride | HCID 98915 | — |
| Produkt | Adamantoyl oxymethyl chloride | HCID 14699931 | — |
Reaktionsschritte
DBU (1,8-diazabicyclo[5.4.0]undec-7-ene; 1.53 g, 10 mmol) was added to a suspension of PMEA (1.365 g, 5 mmol) in DMF (25 mL). Adamantoyl oxymethyl chloride (5.72 g, 25 mmol) in DMF (25 mL) was added to the reaction mixture which was then stirred for four days at room temperature and the volatiles were removed under vacuum. The crude product obtained after removal of the solvent was loaded onto a silica gel column and washed with 3% MeOH/CH2Cl2 to remove nonpolar impurities. 1 g (30%) of bis(adamantoyl oxymethyl)PMEA ester was eluted in 8% MeOH/CH2 Cl2. Adamantoyl oxymethyl chloride was obtained by conversion of 1-adamantanecarbonyl chloride (Aldrich No. 11,772-2) with (CH2 O)n /ZnCl2 and has been described (Bodor, et al J Med Chem (1980) 23 :474-480).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05798340 |
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| Quelldatensatz | uspto-grants-1998_08 |
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| ORD ID | ord-31098abd78524d2eaac7a12440df0b65 |
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| Quellennotiz | uspto-grants-1998_08 |
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