Reaktionsgleichung
[CH3:1][NH:2][CH2:3][CH:4]1[C:16]2C3C(=CC=CC=3)N[C:8]=2[S:7]CC1.C([N:19]([CH2:22][CH3:23])[CH2:20][CH3:21])C.[C:24]([O:28][C:29](SC1N=C(C)C=C(C)N=1)=[O:30])([CH3:27])([CH3:26])[CH3:25].O1[CH2:44][CH2:43][CH2:42][CH2:41]1>>[C:24]([O:28][C:29]([N:2]([CH2:3][CH:4]1[C:23]2[C:21]3[C:20](=[CH:41][CH:42]=[CH:43][CH:44]=3)[NH:19][C:22]=2[S:7][CH2:8][CH2:16]1)[CH3:1])=[O:30])([CH3:27])([CH3:26])[CH3:25]Komponenten
5
Versuchsvorschrift
To a solution of 4-methylaminomethyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole (4.41 g) in tetrahydrofuran (50 ml) are added triethylamine (4 ml) and 2-(t-butoxycarbonylthio)-4,6-dimethylpyrimidine (4.76 l g) successively at room temperature. The mixture is stirred at room temperature for 2.5 hours and evaporated to remove the solvent. The residue is extracted with chloroform after addition of water. The extract is washed, dried and evaporated to give crude crystals. Recrystallization from acetone gives the title compound (5.57 g) melting at 220°-222° C. (decomp.).
Aufarbeitung
- customevaporated
- customto remove the solvent
- extractionThe residue is extracted with chloroform
- additionafter addition of water
- washThe extract is washed
- customdried
- customevaporated
- customto give crude crystals
- customRecrystallization from acetone
Quellen und Nachweise
- ORD-Eintrag
- ord-769f2ca02fde48049ef46625e6e97232
- Quelldatensatz
- uspto-grants-1981_03
- Patentnummer
- US04256640
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