HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 431662Erstellt: 26. Oktober 2026
Boron tribromide → {4-[4-(Pyrrolidine-1-sulfonyl)-piperazin-1-yl]-pyrimidin-2-yl}-methanol
https://huagongshe.com/reaction/431662
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Boron tribromide | HCID 25134 | — |
| Edukt | 2-Methoxymethyl-4-[4-(pyrrolidine-1-sulfonyl)-piperazin-1-yl]-pyrimidine | HCID 22328738 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | {4-[4-(Pyrrolidine-1-sulfonyl)-piperazin-1-yl]-pyrimidin-2-yl}-methanol | HCID 22328774 | — |
Reaktionsschritte
To a solution of 2-methoxymethyl-4-[4-(pyrrolidine-1-sulfonyl)-piperazin-1-yl]-pyrimidine (prepared according to the method of Example 121, Step A, 3.1 g, 9.4 mmol) in dichloromethane (47 mL) was added boron tribromide (1 M in dichloromethane, 19 mL, 18.7 mmol) at 0° C. then stirred at ambient temperature for 2 h. The mixture was washed twice with saturated aqueous sodium bicarbonate, and the organic layer was separated, dried over magnesium sulfate, filtered, and the filtrate was concentrated to give an oil which was crystallized from isopropyl ether to give the title compound as a white solid, 2.43 g (77%). 1H NMR (CDCl3, 300 MHz) δ 1.82 (m, 4H), 3.15 (m, 8H), 3.81 (m, 4H), 4.35 (d, 2H), 4.83 (t, 1H), 6.71 (d, 1H), 8.18 (d, 1H); mp: 128-131° C.; MS (Cl) 328 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06660740B1 |
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| Quelldatensatz | uspto-grants-2003_12 |
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| ORD ID | ord-14596a22ea204ff494fb6831d83fa871 |
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| Quellennotiz | uspto-grants-2003_12 |
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