Hexachloroethane → 6-Fluoro-3-isopropyl-[1,2,4]triazolo[4,3-a]pyridine

HRID 75567

Reaktionsgleichung

Reaktionsgleichung von HRID 75567
[F:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][NH:9][C:10](=O)[CH:11]([CH3:13])[CH3:12])=[N:6][CH:7]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(N(CC)CC)C.ClC(Cl)(Cl)C(Cl)(Cl)Cl>C1COCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:10]([CH:11]([CH3:13])[CH3:12])=[N:9][N:8]=2)[CH:7]=1

Komponenten

6

Versuchsvorschrift

To a solution of Intermediate 1e (1.81 g, 9.18 mmol), triphenylphosphine (4.83 g, 18.4 mmol), and triethylamine (5.12 mL, 36.7 mmol) in THF (25 mL) at 0° C., hexachloroethane (4.36 g, 18.4 mmol) was added in 2 portions at a 1 min intervals. The resulting pale brown solution was allowed to warm to RT then stirred for 2 h. The resulting yellow suspension was filtered, washing with THF (2×25 mL). The combined organics were purified using SCX-2 cartridge (washed with DCM-MeOH (1:1, 100 mL) and MeOH (50 mL), and then the product was eluted with 2M NH3 in MeOH) to give a pale yellow solid (1.60 g, 97%, contaminated with ˜2.5% Ph3P═O). 1H NMR (400 MHz, CDCl3): 1.53 (6H, d), 3.32 (1H, sept), 7.15 (1H, ddd), 7.75 (1H, ddd), 7.84 (1H, m).

Aufarbeitung

  1. filtrationThe resulting yellow suspension was filtered
  2. washwashing with THF (2×25 mL)
  3. customThe combined organics were purified
  4. washwashed with DCM-MeOH (1:1, 100 mL) and MeOH (50 mL)
  5. washthe product was eluted with 2M NH3 in MeOH)
  6. customto give a pale yellow solid (1.60 g, 97%

Quellen und Nachweise

ORD-Eintrag
ord-1af7344cea8a47188f6f1c9e0bb1b5db
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08835431B2

Verknüpfte Notizen

Wird geladen…