2-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenylamino)-6,7-dihydrobenzo[d]thiazol-4(5H)-one → 2-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenylamino)-4-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazol-4-ol

HRID 1803270Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1803270
[C:1]1([Mg]Br)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:9][O:10][C:11]1[CH:12]=[C:13]([NH:23][C:24]2[S:25][C:26]3[CH2:32][CH2:31][CH2:30][C:29](=[O:33])[C:27]=3[N:28]=2)[CH:14]=[CH:15][C:16]=1[N:17]1[CH:21]=[N:20][C:19]([CH3:22])=[N:18]1>C(OCC)C>[CH3:9][O:10][C:11]1[CH:12]=[C:13]([NH:23][C:24]2[S:25][C:26]3[CH2:32][CH2:31][CH2:30][C:29]([C:1]4[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=4)([OH:33])[C:27]=3[N:28]=2)[CH:14]=[CH:15][C:16]=1[N:17]1[CH:21]=[N:20][C:19]([CH3:22])=[N:18]1

Komponenten

4

Versuchsvorschrift

Phenylmagnesium bromide (1.0 M in THF, 0.118 mL, 0.118 mmol) was added to a rt solution of 2-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenylamino)-6,7-dihydrobenzo[d]thiazol-4(5H)-one (14 mg, 0.039 mmol) in diethyl ether (0.13 mL). The reaction was quenched with saturated ammonium chloride and extracted with EtOAc. The organic layer was concentrated in vacuo. The crude product was purified using preparatory TLC (60% acetone/hexanes) to afford 10 mg (53% yield) of the titled compound as a oil. LC-MS (M+H)+ 434.3.

Aufarbeitung

  1. customThe reaction was quenched with saturated ammonium chloride
  2. extractionextracted with EtOAc
  3. concentrationThe organic layer was concentrated in vacuo
  4. customThe crude product was purified

Quellen und Nachweise

ORD-Eintrag
ord-1e79eb94685a40b6ac759108977c3707
Quelldatensatz
uspto-grants-2013_01
Patentnummer
US08349880B2

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