Chlorodimethylaluminum → 4-{4-[(Dimethylamino)sulfonyl]-3-fluorophenoxy)-N-(4-methoxypyridin-2-yl)-2-methyl-1-benzofuran-6-carboxamide

HRID 1177281Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1177281
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([NH2:9])[CH:4]=1.[Al](Cl)(C)C.[CH3:14][N:15]([CH3:42])[S:16]([C:19]1[CH:40]=[CH:39][C:22]([O:23][C:24]2[C:29]3[CH:30]=[C:31]([CH3:33])[O:32][C:28]=3[CH:27]=[C:26]([C:34](OCC)=[O:35])[CH:25]=2)=[CH:21][C:20]=1[F:41])(=[O:18])=[O:17]>ClCCCl.C(Cl)Cl>[CH3:42][N:15]([CH3:14])[S:16]([C:19]1[CH:40]=[CH:39][C:22]([O:23][C:24]2[C:29]3[CH:30]=[C:31]([CH3:33])[O:32][C:28]=3[CH:27]=[C:26]([C:34]([NH:9][C:5]3[CH:4]=[C:3]([O:2][CH3:1])[CH:8]=[CH:7][N:6]=3)=[O:35])[CH:25]=2)=[CH:21][C:20]=1[F:41])(=[O:17])=[O:18]

Komponenten

6

Edukt 3

HCID 79147ChlorodimethylaluminumHCID 108987152-Amino-4-MethoxypyridineHCID 59560433Ethyl 4-{4-[(dimethylamino)sulfonyl]-3-fluorophenoxy}-2-methyl-1-benzofuran-6-carboxylate

Produkt 1

HCID 595604504-{4-[(Dimethylamino)sulfonyl]-3-fluorophenoxy)-N-(4-methoxypyridin-2-yl)-2-methyl-1-benzofuran-6-carboxamideAusbeute 93 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 111,2-DichloroethaneLösungsmittelHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 4-methoxypyridin-2-amine (295 mg, 2.37 mmol) in DCE at 0° C. was added Al(CH3)2Cl (3.0 mL, 1.0M) drop wise, and the reaction was stirred for 20 minutes at room temperature. Ethyl 4-{4-[(dimethylamino)sulfonyl]-3-fluorophenoxy}-2-methyl-1-benzofuran-6-carboxylate (100 mg, 0.24 mmol) was then added and the reaction was stirred at room temperature for an additional 14 hours. The sample was diluted with CH2Cl2 and quenched with potassium sodium tartrate tetrahydrate (20% w/w) (1 mL). The organic layer was washed with brine and dried over Na2SO4 and concentrated under reduced pressure. The crude sample was introduced into a silica gel column and eluted with MeOH/CHCl3 (5/95-10/90) to provide the product (110 mg, 93% yield) as white solid. 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 2.49 (s, 3 H) 2.84 (d, J=1.51 Hz, 6 H) 3.91 (s, 3 H) 6.26 (s, 1 H) 6.64 (dd, J=5.75, 2.35 Hz, 1 H) 6.71-6.91 (m, 2 H) 7.52 (s, 1 H) 7.81 (t, J=8.29 Hz, 1 H) 7.91 (s, 1 H) 8.01 (s, 1 H) 8.09 (d, J=5.84 Hz, 1 H) 8.59 (s, 1 H); MS (ESI, pos): 500.

Aufarbeitung

  1. stirringthe reaction was stirred at room temperature for an additional 14 hours
  2. customquenched with potassium sodium tartrate tetrahydrate (20% w/w) (1 mL)
  3. washThe organic layer was washed with brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under reduced pressure
  6. additionThe crude sample was introduced into a silica gel column
  7. washeluted with MeOH/CHCl3 (5/95-10/90)

Quellen und Nachweise

ORD-Eintrag
ord-7273af1d2198447eb49b39014b45ae6d
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07842713B2

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