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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2284706Erstellt: 25. Oktober 2026

1,1'-(Azodicarbonyl)dipiperidine → HCID 90052119, Verbindung

https://huagongshe.com/reaction/2284706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Edukt3-Nitrobenzene-1-thiolHCID 243576—
EduktHCID 90052116HCID 90052116—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTributylphosphineHCID 13831—
ProduktHCID 90052119HCID 9005211963,5%

Reaktionsschritte

To a solution of (2-((3-fluorophenyl)amino)-4-(propylamino)pyrimidin-5-yl)methanol (E13, 20 mg) and 3-nitrothiophenol (17 mg) in tetrahydrofuran (1 mL), tributylphosphine (36 μL) and 1,1′-(azodicarbonyl)dipiperidine (28 mg) were added under ice cooling, and the mixture was stirred at room temperature for 6 hours and 30 minutes. To the reaction mixture, tributylphosphine (36 μL) and 1,1′-(azodicarbonyl)dipiperidine (28 mg) were added at room temperature, and the mixture was stirred at the same temperature for 8 hours and 30 minutes. The solvent was evaporated under reduced pressure, and then the obtained residue was purified by basic silica gel column chromatography (eluent, 88 to 40% hexane in ethyl acetate) to obtain N2-(3-fluorophenyl)-5-(((3-nitrophenyl)thio)methyl)-N4-propylpyrimidine-2,4-diamine (E19, 19 mg) as yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09145415B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-20c14a64133e4d859015f1104817bb2c
Quellennotizuspto-grants-2015_09