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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507546Erstellt: 25. Oktober 2026

Diisopropylethylamine → HCID 60204370, Verbindung

https://huagongshe.com/reaction/507546

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-(2-Aminoethyl)-5,5-dimethylimidazolidine-2,4-dioneHCID 57428804—
Edukt2-(5-Bromo-2-(methylsulfonyl)pyrimidin-4-yl)thiazolo[5,4-c]pyridineHCID 60204372—
LösungsmittelIsopropanolHCID 3776—
ProduktHCID 60204370HCID 602043705%

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

A microwave tube was charged with 2-(5-bromo-2-(methylsulfonyl)pyrimidin-4-yl)thiazolo[5,4-c]pyridine (300 mg, 0.81 mmol), 1-(2-Aminoethyl)-5,5-dimethyl-imidazolidine-2,4-dione (138 mg, 0.81 mmol), isopropanol (3 mL) and N,N-diisopropylethylamine (0.21 mL, 1.21 mmol). The vessel was sealed and heated in a microwave reactor at 160° C. for 1000 seconds. The resulting solid was filtered off and washed with methanol (4×10 mL). The solid was then dissolved in dimethylsulfoxide (4 mL) and purified by reverse phase HPLC. Product fractions were combined and loaded onto an SCX cartridge, washed with methanol (4 mL), then free based and eluted with 2 M ammonia in methanol (4 mL). The solvent was evaporated in vacuo to yield 1-(2-(5-bromo-4-(thiazolo[5,4-c]pyridin-2-yl)pyrimidin-2-ylamino)ethyl)-5,5-dimethylimidazolidine-2,4-dione (17 mg, 5%) as a yellow amorphous solid. 1H NMR δ (d6-DMSO, 400 MHz) 1.50 (s, 6H), 3.67 (br. s., 2H), 3.75 (br. s., 2H), 4.32 (br. s., 1H), 6.89 (s, 1H), 7.49 (s, 1H), 8.33 (d, J=5.5 Hz, 1H), 8.91 (d, J=5.1 Hz, 1H), 9.71 (s, 1H): HRMS (M+H)+ Calcd. C17H16BrN7O2S 462.0348. found 462.0339.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07786132B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-7de86fabc66643d6a25d9720ab56c7bc
Quellennotizuspto-grants-2010_08