Ammonia → 6-Fluoro-3-((S)-1,4,4-trimethyl-pyrrolidin-2-yl)-[1,2,4]triazolo[4,3-a]pyridine

HRID 2285117Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2285117
[F:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][NH:9][C:10]([C@@H:12]2[CH2:16][C:15]([CH3:18])([CH3:17])[CH2:14][N:13]2[CH3:19])=O)=[N:6][CH:7]=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CCN(CC)CC.ClC(Cl)(Cl)C(Cl)(Cl)Cl.N>C1COCC1.CO.C(Cl)Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:10]([C@@H:12]3[CH2:16][C:15]([CH3:18])([CH3:17])[CH2:14][N:13]3[CH3:19])=[N:9][N:8]=2)[CH:7]=1

Komponenten

9

Versuchsvorschrift

To a solution of Intermediate 87b (950 mg, 3.57 mmol), Ph3P (1.87 g, 7.14 mmol) and Et3N (1.44 g, 14.28 mmol) in THF (40 mL) was added hexachloroethane (1.65 g, 7.14 mmol) and the mixture stirred at RT for 20 h. The reaction mixture was applied to an SCX-2 cartridge (70 g) and washed with MeOH. The product was eluted with 2M NH3 in MeOH; concentration in vacuo gave a residue. FCC, using 0-10% [2M NH3 in MeOH] in DCM gave the title compound as a clear oil (750 mg, 84%). 1H NMR (400 MHz, CDCl3): 1.22 (3H, s), 1.24 (3H, s), 1.84 (1H, dd, J 12.7, 10.8), 2.04 (1H, dd, J 12.4, 7.4), 2.16 (3H, s), 2.25 (1H, d J, 9.1), 3.04 (1H, d, J 9.3), 4.22 (1H, dd, J 10.0, 7.6), 7.14-7.23 (1H, m), 7.69-7.77 (1H, m), 8.75-8.80 (1H, m).

Aufarbeitung

  1. washwashed with MeOH
  2. washThe product was eluted with 2M NH3 in MeOH
  3. concentrationconcentration in vacuo
  4. customgave a residue

Quellen und Nachweise

ORD-Eintrag
ord-36c2a2e594084b20af0363887c42895f
Quelldatensatz
uspto-grants-2015_09
Patentnummer
US09145413B2

Notizen zur Reaktion

Wird geladen…