Trifluoroacetic acid → 5,6-Dihydrophenanthridine

HRID 2181836Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2181836
[CH2:1]([C:3]1[N:4]=[C:5]2[C:10](=[C:11]3[C:16]=1[CH:15]=[C:14]([F:17])[CH:13]=[CH:12]3)[CH:9]=[CH:8][CH:7]=[CH:6]2)[CH3:2].[BH4-].[Na+].FC(F)(F)C(O)=O.C1C=CC2C3C=CC=CC=3NCC=2C=1.C(N(CC)CC)C.[CH3:48][O:49][C:50]1[CH:55]=[CH:54][C:53]([S:56](Cl)(=[O:58])=[O:57])=[CH:52][C:51]=1[CH3:60]>O1CCCC1.ClCCl>[CH:14]1[CH:13]=[CH:12][C:11]2[C:10]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[NH:4][CH2:3][C:16]=2[CH:15]=1.[CH2:1]([CH:3]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([F:17])[CH:15]=2)[C:10]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[N:4]1[S:56]([C:53]1[CH:54]=[CH:55][C:50]([O:49][CH3:48])=[C:51]([CH3:60])[CH:52]=1)(=[O:58])=[O:57])[CH3:2]

Komponenten

10

Edukt 6

HCID 6422Trifluoroacetic acidHCID 8471TriethylamineHCID 2199665,6-DihydrophenanthridineHCID 4311764Sodium borohydrideHCID 159153174-Methoxy-3-methylbenzene-1-sulfonyl chlorideHCID 22482260HCID 22482260, Verbindung

Produkt 2

HCID 2199665,6-DihydrophenanthridineHCID 22482394HCID 22482394, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

The intermediate dihydrophenanthridine was prepared from 6-ethyl-8-fluoro-phenanthridine, (Example 40, Step b, 0.79 g, 3.48 mmol), by treatment with sodium borohydride (0.79 g, 21 mmol) and trifluoroacetic acid (1.1 mL, 14 mmol) in tetrahydrofuran (18 mL). In a separate, second step, the dihydrophenanthridine was treated with triethylamine (0.8 mL, 6 mmol) and 4-methoxy-3-methylbenzenesulfonyl chloride (0.66 g, 3.0 mmol, 2 equivalents) in dichloromethane (5 mL) according to the procedure and in the same manner as described in Example 32, Method A, Step d. The crude product was purified by flash column chromatography on silica gel, eluting with a mixture of ethyl acetate-hexane (1:19 to 3:7 gradient), to yield 6-ethyl-8-fluoro-5-[(4-methoxy-3-methylphenyl)sulfonyl]-5,6-dihydrophenanthridine as a homogeneous, white solid (0.57 g, 92% from the dihydrophenanthridine), m.p. 140° C.;

Aufarbeitung

  1. customThe crude product was purified by flash column chromatography on silica gel
  2. washeluting with a mixture of ethyl acetate-hexane (1:19 to 3:7 gradient)

Quellen und Nachweise

ORD-Eintrag
ord-48ca3ab43e1a4464b8d6d3c21c51e4a1
Quelldatensatz
uspto-grants-2005_05
Patentnummer
US06894061B2

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