Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][N:4]=[C:3]([C:7]([OH:9])=O)[C:2]=1[C:10]([OH:12])=O.C1CN([P+](ON2N=[N:37][C:32]3[CH:33]=CC=C[C:31]2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.C1C=CC2N([OH:55])N=NC=2C=1.CN1C[CH2:61][O:60]CC1.[NH2:63][C:64]([CH3:69])([CH2:67][OH:68])[CH2:65][OH:66]>CN(C=O)C.C(O)(C(F)(F)F)=O.CC#N>[OH:66][CH2:65][C:64]([NH:63][C:7]([C:3]1[C:2]([C:10]([NH:37][C:32]([CH3:31])([CH2:33][OH:55])[CH2:61][OH:60])=[O:12])=[N:1][CH:6]=[CH:5][N:4]=1)=[O:9])([CH3:69])[CH2:67][OH:68]Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
Pyrazine-2,3-dicarboxylic acid (34 mg, 0.2 mmol), PyBOP (229 mg, 0.44 mmol), HOBt (60 mg, 0.44 mmol) and NMM (0.7 mL, 0.64 mmol) were dissolved in DMF (2 mL) and allowed to react for 10 min. 2-Amino-2-methyl-1,3-propanediol (46 mg, 0.44 mmol) was then added and stirring was continued overnight. The entire reaction mixture was then fractionated on a RP-HPLC column (Vydac 218TP1022, 22×250 mm, 10 mL/min, 0 to 15% MeCN in 0.1% aq CF3COOH over 40 min). Appropriate fractions were pooled, rechromatographed and lyophilised to yield the pure title compound. Alternatively, the title compound was synthesised as follows: dimethylpyrazine-2,3-dicarboxylate (1.5 g, 7.7 mmol) and 2-amino-2-methyl-1,3-propanediol (1.6 g, 15.4 mmol) in absolute ethanol (5 mL) were heated under reflux during 4 hours. The reaction mixture was then cooled and the solvent was removed under reduced pressure. The residue was chromatographed on a flash silica gel column using CHCl3 /MeOH (4:1) as the eluant. Solvents were removed in vacua and the pure title compound (2.2 g, 85%) was obtained after recrystallisation from isopropanol/hexane.
Aufarbeitung
- customto react for 10 min
- customThe entire reaction mixture
- customrechromatographed
Quellen und Nachweise
- ORD-Eintrag
- ord-da604404412144d49af83901be92b4cb
- Quelldatensatz
- uspto-grants-2000_09
- Patentnummer
- US06124298
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