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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 220358Erstellt: 23. Oktober 2026

Potassium Carbonate → HCID 58180582, Verbindung

https://huagongshe.com/de/reaction/220358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktBenzoyl isothiocyanateHCID 68284—
Edukt2-Bromo-1-(2-pyridinyl)-1-ethanone hydrobromideHCID 2776231—
Edukt4-amino-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamideHCID 58180503—
LösungsmittelAcetoneHCID 180—
ProduktHCID 58180582HCID 5818058210%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A solution of 4-amino-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (example 1J, 70 mg, 0.21 mmol) and benzoyl isothiocyanate (36 μl, 0.27 mmol) in acetone (1 ml) was stirred at room temperature for 1.5 h. The solvent was removed in vacuo, the residue was taken up in EtOH (1.5 ml), and K2CO3 (40 mg, 0.290 mmol) was added. The reaction was heated at 60° C. for 3 h. Upon cooling to room temperature, 2-bromo-1-(pyridin-2-yl)ethanone, hydrobromide (139.4 mg, 0.50 mmol) was added and the reaction heated at 80° C. for 24 h. The reaction mixture was cooled to room temperature and concentrated. The residue was purified by silica gel chromatography (0-7% MeOH/dichloromethane). Re-purification by preparative HPLC provided 10.2 mg (10% yield) of N,N-dicyclopropyl-6-ethyl-1-methyl-4-(4-(pyridin-2-yl)thiazol-2-ylamino)-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide as a brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202881B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-784294f13ca14d49a5ece0fc2b4d2b57
Quellennotizuspto-grants-2012_06