Boron trifluoride etherate → 1-Methyl-1,4-dihydro-2H-3-thia-2,4,5-triaza-phenanthrene 3,3-dioxide

HRID 513687Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 513687
[CH2:1](OCC)C.FB(F)F.[CH:10]1[C:23]2[CH:22]=[CH:21][C:20]3[C:15](=[N:16][CH:17]=[CH:18][CH:19]=3)[C:14]=2[NH:13][S:12](=[O:25])(=[O:24])[N:11]=1.C[Li]>C1COCC1>[CH3:1][CH:10]1[C:23]2[CH:22]=[CH:21][C:20]3[C:15](=[N:16][CH:17]=[CH:18][CH:19]=3)[C:14]=2[NH:13][S:12](=[O:25])(=[O:24])[NH:11]1

Komponenten

5

Versuchsvorschrift

Ethoxyethane—trifluoroborane (1:1; 32.3 μl, 0.26 mmol) was added dropwise to a solution of 4H-3-thia-2,4,5-triaza-phenanthrene 3,3-dioxide 406 (60 mg, 0.26 mmol) in dry THF (3 ml) under an atmosphere of N2. The mixture was stirred at room temperature for 1 h and then cooled to −78° C. Methyllithium (1.6M in Et2O; 1.61 ml, 2.57 mmol) was added dropwise and the mixture was stirred −78° C. for 1 h. The reaction was quenched with sat NH4Cl (2 ml) at -78° C. and the mixture was warmed to room temperature. The mixture was extracted with EtOAc and the residue was purified by preparative HPLC (acidic conditions 1) to give the title compound (18 mg, 28%).

Aufarbeitung

  1. temperaturecooled to −78° C
  2. stirringthe mixture was stirred −78° C. for 1 h
  3. customThe reaction was quenched with sat NH4Cl (2 ml) at -78° C.
  4. temperaturethe mixture was warmed to room temperature
  5. extractionThe mixture was extracted with EtOAc
  6. customthe residue was purified by preparative HPLC (acidic conditions 1)

Quellen und Nachweise

ORD-Eintrag
ord-0bedb2d0d9f34f26a43338d626b5b1a0
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09102688B2

Notizen zur Reaktion

Wird geladen…