4-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenol → 4-{[(6R)-3-fluoro-6-methylphenanthridin-5(6H)-yl]carbonyl}phenol

HRID 731991Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 731991
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6]3[C:11]([CH:12]([CH3:25])[N:13]([C:16]([C:18]4[CH:23]=[CH:22][C:21]([OH:24])=[CH:20][CH:19]=4)=[O:17])[C:14]=2[CH:15]=1)=[CH:10][CH:9]=[CH:8][CH:7]=3>C(Cl)(Cl)Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6]3[C:11]([C@@H:12]([CH3:25])[N:13]([C:16]([C:18]4[CH:19]=[CH:20][C:21]([OH:24])=[CH:22][CH:23]=4)=[O:17])[C:14]=2[CH:15]=1)=[CH:10][CH:9]=[CH:8][CH:7]=3

Komponenten

3

Edukt 1

HCID 115807984-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenol

Produkt 1

HCID 116956764-{[(6R)-3-fluoro-6-methylphenanthridin-5(6H)-yl]carbonyl}phenol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Versuchsvorschrift

The enantiomers of 4-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenol (720 mg, 2.16 mmol) were separated by automated, on-column solvent change, preparative, normal phase, chiral chromatography on a Chiralpak AD (20 mm×250 mm) column eluting with 35% hexane in ethanol at a flow rate of 15 mL/min with. The fractions containing the first peak were combined and concentrated in vacuo, to provide one peak (99.9%) with a retention time of 3.620 minutes was isolated as a white solid (318 mg, 88% based upon a 1:1 ratio of enantiomers with a theoretical maximum amount of 360 mg). mp 235.7-236.8° C.; [α]D25=−648° (c=0.010 g/mL, CHCl3); 1H NMR (400 MHz, DMSO-d6) δ ppm 1.21 (d, J=6.98 Hz, 3 H) 5.68 (q, J=6.73 Hz, 1 H) 6.56 (dd, J=10.48, 2.46 Hz, 1 H) 6.70 (d, J=8.79 Hz, 2 H) 7.06 (td, J=8.60, 2.72 Hz, 1 H) 7.16 (m, 2 H) 7.35 (m, 1 H) 7.42 (m, 2 H) 7.98 (td, J=8.73, 7.11 Hz, 2 H) 10.04 (s, 1H) MS (ESI) m/z 334 ([M+H]+); MS (ESI) m/z 332 ([M−H]−).

Aufarbeitung

  1. washpreparative, normal phase, chiral chromatography on a Chiralpak AD (20 mm×250 mm) column eluting with 35% hexane in ethanol at a flow rate of 15 mL/min with
  2. additionThe fractions containing the first peak
  3. concentrationconcentrated in vacuo
  4. customto provide one peak (99.9%) with a retention time of 3.620 minutes
  5. customwas isolated as a white solid (318 mg, 88%

Quellen und Nachweise

ORD-Eintrag
ord-1ae24a6d6f864c8e871db2bc071a56ff
Quelldatensatz
uspto-grants-2009_09
Patentnummer
US07585871B2

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