HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 657748Erstellt: 26. Oktober 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 5-(Azidomethyl)-2-methylpyrimidine
https://huagongshe.com/reaction/657748
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | Diphenylphosphoryl azide | HCID 123414 | — |
| Edukt | (2-Methylpyrimidin-5-yl)methanol | HCID 14686706 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-(Azidomethyl)-2-methylpyrimidine | HCID 54595022 | — |
Reaktionsschritte
A solution of (2-methylpyrimidin-5-yl)methanol (0.82 g, 6.6 mmol) in toluene (30 mL) and methylene chloride (40 mL) at 0° C. was treated with diphenylphosphonic azide (2.8 mL, 13 mmol) followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (2.0 mL, 13 mmol) and stirred at 0° C. for 2 h. After being further stirred at rt for 16 h, the reaction mixture was diluted with water (50 mL) and methylene chloride (50 mL). The organic layer was separated and washed with brine, dried (Mg2SO4), filtered, and concentration. The residue was purified by silica gel column to yield a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08076345B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-3d3d0b07d9b84da49fe303d46f429500 |
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| Quellennotiz | uspto-grants-2011_12 |
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