Ethyl Acetate → {5-[(6-Methyl-4'-trifluoromethylbiphenyl-2-carbonyl)-amino]-indan-2-yl}-carbamic acid tert-butyl ester

HRID 1531306Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1531306
[C:1]([O:5][C:6](=[O:8])[NH2:7])([CH3:4])([CH3:3])[CH3:2].C([N:12]([CH:15]([CH3:17])[CH3:16])CC)(C)C.[CH3:18][C:19]1[CH:20]=[CH:21][CH:22]=[C:23]([C:35](Cl)=[O:36])[C:24]=1[C:25]1[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:33])[F:32])=[CH:27][CH:26]=1.C(O[CH2:42][CH3:43])(=O)C>C(Cl)Cl>[C:1]([O:5][C:6](=[O:8])[NH:7][CH:43]1[CH2:42][C:3]2[C:1](=[CH:2][CH:17]=[C:15]([NH:12][C:35]([C:23]3[C:24]([C:25]4[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:33])[F:32])=[CH:27][CH:26]=4)=[C:19]([CH3:18])[CH:20]=[CH:21][CH:22]=3)=[O:36])[CH:16]=2)[CH2:4]1)([CH3:4])([CH3:3])[CH3:2]

Komponenten

6

Versuchsvorschrift

To a solution of 5-amino-indan-2-yl)-carbamic acid tert-butyl ester (12.5 mmol) in methylene chloride (75 mL) is added diisopropylethyl amine (3.3 g, 25 mmol) followed by a solution of 6-methyl-4′-trifluoromethylbiphenyl-2-carboxylic acid chloride in methylene chloride (See Example 14, 12.6 mmol). After stirring 16 h, the reaction mixture is poured into ethyl acetate and washed with 1N HCl, NaHCO3 solution, and brine. The organic layer is dried (MgSO4) and concentrated under reduced pressure to give a solid. Recrystallization from toluene gives {5-[(6-methyl-4′-trifluoromethylbiphenyl-2-carbonyl)-amino]-indan-2-yl}-carbamic acid terf-butyl ester.

Aufarbeitung

  1. washwashed with 1N HCl, NaHCO3 solution, and brine
  2. dry with materialThe organic layer is dried (MgSO4)
  3. concentrationconcentrated under reduced pressure
  4. customto give a solid
  5. customRecrystallization from toluene

Quellen und Nachweise

ORD-Eintrag
ord-9335f3caa7914b8d86d3d86a53dad3e1
Quelldatensatz
uspto-grants-2001_03
Patentnummer
US06197798B1

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