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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60203Erstellt: 23. Oktober 2026

5-(Trifluoromethyl)pyrazin-2-amine → [2-(2,6-Dichloro-benzyl)-thiazolo[5,4-d]pyrimidin-7-yl]-(5-trifluoromethyl-pyrazin-2-yl)-amine

https://huagongshe.com/de/reaction/60203

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-(Trifluoromethyl)pyrazin-2-amineHCID 13341115—
EduktSodium t-butoxideHCID 23676156—
Edukt7-Chloro-2-(2,6-dichloro-benzyl)-thiazolo[5,4-d]pyrimidineHCID 57742463—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
KatalysatorDitert-butyl(cyclopenta-1,3-dien-1-yl)phosphane;iron(2+);(2,3,4,5-tetraphenylcyclopenta-1,4-dien-1-yl)benzeneHCID 12024214—
LösungsmittelTolueneHCID 1140—
Produkt[2-(2,6-Dichloro-benzyl)-thiazolo[5,4-d]pyrimidin-7-yl]-(5-trifluoromethyl-pyrazin-2-yl)-amineHCID 42642035—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a mixture of 7-chloro-2-(2,6-dichloro-benzyl)-thiazolo[5,4-d]pyrimidine (113 mg, 0.34 mmol), 1,2,3,4,5-pentaphenyl-1-(di-t-butylphosphino)ferrocene (49 mg, 0.07 mmol), tris(dibenzylideneacetone)dipalladium (0) (31 mg, 0.03 mmol), and 5-trifluoromethyl-pyrazin-2-ylamine (66 mg, 0.41 mmol) in toluene (3 mL) was added NaOtBu (40 mg, 0.41 mmol) at rt. The mixture was heated to 90° C. under N2. After 18 h, the reaction mixture was cooled and filtered through a pad of diatomaceous earth, eluting with MeOH (30 mL). The filtrate was concentrated and the crude residue was purified using preparative reverse-phase HPLC to afford the title compound a colorless solid (43 mg, 28%). MS (ESI): mass calcd. for C17H9Cl2F3N6S, 455.9; m/z found, 457.0 [M+H]+. 1H NMR ((CD3)250): 10.77 (s, 1H), 9.49 (s, 1H), 8.88-8.87 (m, 1H), 8.75 (s, 1H), 7.59 (d, J=8.0 Hz, 2H), 7.45 (dd, J=8.5, 7.7 Hz, 1H), 4.83 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440978B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-60d87fc246db407c813b239fae238976
Quellennotizuspto-grants-2016_09