Reaktionsgleichung
[C:1]([C:5]1[N:10]=[CH:9][C:8]([C:11]#[N:12])=[CH:7][N:6]=1)([CH3:4])([CH3:3])[CH3:2].Cl.Cl.[NH2:15][C:16]1[CH:17]=[N:18][C:19]([C:23]([CH3:26])([CH3:25])[CH3:24])=[CH:20][C:21]=1N.Cl.Cl.C1(N)C=CC=CC=1N.C(=O)([O-])[O-].[Na+].[Na+].C(=O)=O>C(O)C.O>[C:1]([C:5]1[N:10]=[CH:9][C:8]([C:11]2[NH:15][C:16]3[CH:17]=[N:18][C:19]([C:23]([CH3:25])([CH3:24])[CH3:26])=[CH:20][C:21]=3[N:12]=2)=[CH:7][N:6]=1)([CH3:4])([CH3:2])[CH3:3]Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Preparation analogous to 16), S43, using 16.1 g (100 mmol) of 2-tert-butyl-5-cyanopyrimidine [126230-72-6] and 71.4 g (300 mmol) of 3,4-diamino-6-tert-butylpyridine dihydrochloride (S50) instead of 25.9 g (100 mmol) of 2-N-pivaloylamido-3-cyano-6-tert-butylpyridine (S42) and 90.5 g (500 mmol) of o-phenylenediamine dihydrochloride [615-28-1]. After cooling, the violet melt is dissolved in a mixture of 150 ml of ethanol and 300 ml of water at elevated temperature, and a solution of 25 g of sodium carbonate in 100 ml of water is then added dropwise with vigorous stirring (note: foaming, evolution of carbon dioxide). When the addition is complete, the mixture is stirred for a further 30 min., the brown solid is then filtered off with suction, washed three times with 100 ml of water each time and dried in vacuo. Yield: 23.8 g (77 mmol), 77%. Purity: >95% according to 1H-NMR.
Aufarbeitung
- customPreparation analogous to 16), S43
- temperatureAfter cooling
- additionWhen the addition
- filtrationthe brown solid is then filtered off with suction
- washwashed three times with 100 ml of water each time
- customdried in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-5e49d604c9bd434f8499cee66314e496
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09273080B2
Verknüpfte Notizen
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