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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 467725Erstellt: 25. Oktober 2026

4-Methylmorpholine → HCID 58548177, Verbindung

https://huagongshe.com/reaction/467725

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
Edukt2-(Propan-2-yloxy)ethan-1-amineHCID 533866—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt3-{[6-Cyclopropyl-3-(pyrimidin-5-ylamino)-pyrazine-2-carbonyl]-amino}-isonicotinic acidHCID 70098928—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 58548177HCID 5854817780,4%

Reaktionsschritte

To a stirred mixture of 2-aminoethyl isopropyl ether (25 mg, 242 μmol) and 3-{[6-cyclopropyl-3-(pyrimidin-5-ylamino)-pyrazine-2-carbonyl]-amino}-isonicotinic acid (101 mg, 267 μmol) at rt in THF (5 ml) under an argon atmosphere were added 4-methylmorpholine (123 mg, 134 μl, 1.21 mmol) and HATU (184 mg, 485 μmol). The mixture was heated to reflux and stirring was continued for 1 day. The reaction mixture was concentrated. The crude product was purified by silica gel chromatography using an EtOAc/MeOH gradient as eluent. After trituration with MeOH, the title compound (90 mg, 80%) was obtained as yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08623866B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-b4c10af434614ecbaae0174a684336ff
Quellennotizuspto-grants-2014_01