HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219709Erstellt: 24. Oktober 2026
Sodium Iodide → (S)-Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-2-methyl-propyl ester
https://huagongshe.com/de/reaction/219709
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | (R)-(-)-1-acetoxy-3-bromo-2-methyl-propane | HCID 10420167 | — |
| Edukt | 2-tert-Butyl-4-cyclobutyl-6-(piperazin-1-yl)pyrimidine | HCID 66673390 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (S)-Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-2-methyl-propyl ester | HCID 131729779 | 102,9% |
Reaktionsschritte
3.87 g of 2-tert-butyl-4-cyclobutyl-6-piperazin-1-yl-pyrimidine (14.1 mmol) were stirred in 30 ml of dimethylformamide at room temperature. 3.18 g of triethylamine (63.1 mmol), 0.235 g of sodium iodide (1.57 mmol), 2.96 g of (R)-(−)-1-acetoxy-3-bromo-2-methyl-propane (15.2 mmol) were added and the reaction mixture was stirred for 5 h at 95° C. The dimethylformamide was evaporated under reduced pressure. The residue was partitioned between 100 ml of dichloromethane and 100 ml of water. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure to give a brownish oil (5.64 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08202868B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-8ad93d4589f643a19d73bbb7382181e8 |
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| Quellennotiz | uspto-grants-2012_06 |
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