Ethyl Acetate → 1-(5-Methyl-1H-indazol-4-ylamino)-6-fluoro-4,4-dimethyl-2-(trifluoromethyl)-1,2,3,4-tetrahydro-naphthalene-2,5-diol

HRID 1444490Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1444490
[F:1][C:2]([F:31])([F:30])[C:3]([CH:18]=[N:19][C:20]1[C:28]([CH3:29])=[CH:27][CH:26]=[C:25]2[C:21]=1[CH:22]=[N:23][NH:24]2)([OH:17])[CH2:4][C:5]([C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[C:9]=1[O:15]C)([CH3:7])[CH3:6].B(Br)(Br)Br.C(=O)(O)[O-].[Na+].C(OCC)(=O)C>ClCCl>[CH3:29][C:28]1[C:20]([NH:19][CH:18]2[C:13]3[CH:12]=[CH:11][C:10]([F:14])=[C:9]([OH:15])[C:8]=3[C:5]([CH3:6])([CH3:7])[CH2:4][C:3]2([C:2]([F:31])([F:30])[F:1])[OH:17])=[C:21]2[C:25](=[CH:26][CH:27]=1)[NH:24][N:23]=[CH:22]2

Komponenten

6

Edukt 4

HCID 8857Ethyl AcetateHCID 25134Boron tribromideHCID 516892Sodium BicarbonateHCID 686820761,1,1-Trifluoro-4-(3-fluoro-2-methoxyphenyl)-4-methyl-2-[(5-methyl-1H-indazol-4-ylimino)-methyl]-pentan-2-ol

Produkt 1

HCID 865999241-(5-Methyl-1H-indazol-4-ylamino)-6-fluoro-4,4-dimethyl-2-(trifluoromethyl)-1,2,3,4-tetrahydro-naphthalene-2,5-diol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

1,1,1-Trifluoro-4-(3-fluoro-2-methoxyphenyl)-4-methyl-2-[(5-methyl-1H-indazol-4-ylimino)-methyl]-pentan-2-ol (150 mg, 0.34 mmol) is mixed with boron tribromide (3.40 ml of a 1 M solution in dichloromethane, 3.4 mmol) at room temperature. After 4 hours at room temperature, the reaction mixture is allowed to stand overnight at −30° C., then saturated sodium bicarbonate solution and ethyl acetate are added. It is extracted with ethyl acetate, and the combined organic phases are washed with saturated sodium chloride solution and dried on sodium sulfate. After the solvent is removed in a vacuum as well as purification by means of preparative thin-layer chromatography on silica gel with hexane/ethyl acetate (50% ethyl acetate), 56 mg (39% of theory) of the product is obtained.

Aufarbeitung

  1. waitto stand overnight at −30° C.
  2. extractionIt is extracted with ethyl acetate
  3. washthe combined organic phases are washed with saturated sodium chloride solution
  4. customdried on sodium sulfate
  5. customAfter the solvent is removed in a vacuum as
  6. customwell as purification by means of preparative thin-layer chromatography on silica gel with hexane/ethyl acetate (50% ethyl acetate), 56 mg (39% of theory) of the product
  7. customis obtained

Quellen und Nachweise

ORD-Eintrag
ord-d1b5e02f9bae49d3b6ec56149838ce6d
Quelldatensatz
uspto-grants-2010_02
Patentnummer
US07662821B2

Notizen zur Reaktion

Wird geladen…