Water → Ispronicline hemigalactarate

HRID 489763

Reaktionsgleichung

[CH3:1][NH:2][C@H:3]([CH2:5]/[CH:6]=[CH:7]/[C:8]1[CH:9]=[N:10][CH:11]=[C:12]([O:14][CH:15]([CH3:17])[CH3:16])[CH:13]=1)[CH3:4].[O:18]=[C:19]([OH:31])[C@@H:20]([C@H:22]([C@H:24]([C@@H:26]([C:28]([OH:30])=[O:29])[OH:27])[OH:25])[OH:23])[OH:21].O>C(O)C>[O:18]=[C:19]([OH:31])[C@@H:20]([C@H:22]([C@H:24]([C@@H:26]([C:28]([OH:30])=[O:29])[OH:27])[OH:25])[OH:23])[OH:21].[CH3:1][NH:2][C@H:3]([CH2:5]/[CH:6]=[CH:7]/[C:8]1[CH:9]=[N:10][CH:11]=[C:12]([O:14][CH:15]([CH3:17])[CH3:16])[CH:13]=1)[CH3:4].[CH3:1][NH:2][C@H:3]([CH2:5]/[CH:6]=[CH:7]/[C:8]1[CH:9]=[N:10][CH:11]=[C:12]([O:14][CH:15]([CH3:17])[CH3:16])[CH:13]=1)[CH3:4]

Komponenten

Reaktionsbedingungen

Temperatur: 70 °C

Versuchsvorschrift

(2S)-(4E)-N-Methyl-5-(5-isopropoxy-3-pyridyl)-4-penten-2-amine (2.00 g, 8.55 mmol) was dissolved in ethyl alcohol (20 mL), assisted by warming to 70° C. The warm solution was treated with galactaric acid (900 mg, 4.27 mmol) in one portion, followed by the dropwise addition of water (0.5 mL). The solution was filtered while hot to remove some insoluble material. The filtrate was allowed to cool to ambient temperature. The resulting crystals were filtered, washed with anhydrous diethyl ether, and dried under vacuum at 40° C. to yield a white, crystalline powder (750 mg, 26.0%), mp 140-143° C.

Aufarbeitung

filtrationThe solution was filtered while hot
customto remove some insoluble material
temperatureto cool to ambient temperature
filtrationThe resulting crystals were filtered
washwashed with anhydrous diethyl ether
customdried under vacuum at 40° C.

Quellen und Nachweise

ORD-Eintrag: ord-fa05ee349f494d538662a1cd68c3c4a7
Quelldatensatz: uspto-grants-2005_12
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US06979695B2

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