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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1966686Erstellt: 24. Oktober 2026

Sodium Thiosulfate → HCID 53236719, Verbindung

https://huagongshe.com/de/reaction/1966686

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ThiosulfateHCID 24477—
EduktPotassium hydroxy sulfiteHCID 23707502—
Edukt4-(2-amino-pyrimidin-5-yl)-N1-tert-butyl-benzene-1,2-diamineHCID 58541899—
Edukt2-(2,4-Dimethyl-thiazol-5-yl)-5-methoxy-benzaldehydeHCID 58542002—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 53236719HCID 5323671943%

Reaktionsschritte

To a solution of 4-(2-amino-pyrimidin-5-yl)-N1-tert-butyl-benzene-1,2-diamine (100 mg, 0.39 mmol) in DMF (5 mL) is added 2-(2,4-dimethyl-thiazol-5-yl)-5-methoxy-benzaldehyde (144 mg, 0.58 mmol) at room temperature. Oxone (239 mg, 0.39 mmol) in H2O (1 mL) is added and the solution is stirred for 4 hours. Saturated sodium thiosulfate solution (5 mL) is added and the mixture is extracted with EtOAc (3×10 mL) and H2O (10 mL). The combined organic layer is dried with MgSO4 and is filtered. The filtrate is concentrated and the residue is purified by silica gel flash column chromatography eluting with 10% MeOH in CH2Cl2 to afford the title compound (81 mg, 43%) as a pale brown foam. LCMS (ESMS): m/z 485.72 (M++1)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08420655B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-cd15a7c7d9474ab8961fb4ebf8bd6bbd
Quellennotizuspto-grants-2013_04