Tert-Butylamine → Urea, N-(1,1-dimethylethyl)-N(sup 1)-(5-(2-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl)-

HRID 848119Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 848119
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]([CH3:12])[C:10](=[O:13])[CH2:9][N:8]=[C:7]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[F:20])[C:6]=2[CH:21]=1.[C:22]([NH2:26])([CH3:25])([CH3:24])[CH3:23].[CH2:27](Cl)Cl.[OH2:30]>>[C:22]([NH:26][C:27]([NH:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]([CH3:12])[C:10](=[O:13])[CH2:9][N:8]=[C:7]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[F:20])[C:6]=2[CH:21]=1)=[O:30])([CH3:25])([CH3:24])[CH3:23]

Komponenten

4

Versuchsvorschrift

A dichloroethane solution of [5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]isocyanate, obtained as described in paragraph (a) of Example 1 from 4.2 g (0.015 M) of 7-amino-5-(o-fluorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one, is treated with excess tert.butylamine. After concentration of the mixture, the residue is taken up in methylene chloride/water and the methylene chloride solution is washed several times with water. After drying the organic phase over sodium sulphate, the sodium sulphate is filtered off and the methylene chloride is evaporated off. The residue is purified on a silica gel column (150 g of SiO2) using 40% ethyl acetate in methylene chloride as the eluting agent and crystallised from ethanol/petroleum ether. There is obtained 1-tert.butyl-3-[5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]urea which melts at 210° C. with decomposition.

Aufarbeitung

  1. washthe methylene chloride solution is washed several times with water
  2. dry with materialAfter drying the organic phase over sodium sulphate
  3. filtrationthe sodium sulphate is filtered off
  4. customthe methylene chloride is evaporated off
  5. customThe residue is purified on a silica gel column (150 g of SiO2)
  6. customcrystallised from ethanol/petroleum ether

Quellen und Nachweise

ORD-Eintrag
ord-ebb97e2471cd44c592cea023ebaa212b
Quelldatensatz
uspto-grants-1981_10
Patentnummer
US04294758

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