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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 869063Erstellt: 24. Oktober 2026

Di-tert-butyl azodicarboxylate → Di-tert-butyl 1-(2,4-dimethoxypyrimidin-5-yl)hydrazine-1,2-dicarboxylate

https://huagongshe.com/de/reaction/869063

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDi-tert-butyl azodicarboxylateHCID 97268—
Edukt5-Bromo-2,4-dimethoxypyrimidineHCID 255719—
EduktHCID 178461733HCID 178461733—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktDi-tert-butyl 1-(2,4-dimethoxypyrimidin-5-yl)hydrazine-1,2-dicarboxylateHCID 90303215100%

Reaktionsschritte

Isopropylmagnesium chloride-lithium chloride complex (1.3 M in THF, 18.3 mL, 23.7 mmol) was added dropwise to a cold (0° C.) solution of 5-bromo-2,4-dimethoxypyrimidine (4 g, 18.3 mmol) in THF (50 mL), under argon. The reaction mixture was allowed to warm to rt and stirred for 1 h at this temperature. Di-tertbutyl azodicarboxylate (4.2 g, 18.3 mmol) was added portionwise. The reaction mixture was stirred for 1 h at rt, diluted with brine, and extracted with EtOAc. The organic layers were combined, washed with brine, dried (Na2SO4), and concentrated. The residue was purified by silica gel column chromatography (hexane/EtOAc, 9:1→7.3) to provide 6.78 g of the title compound. tR: 1.08 min (LC-MS 4); ESI-MS: 371.3 [M+H]+ (LC-MS 4); Rf=0.55 (hexane/EtOAc, 1:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08969341B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-0a93f58261644c23aaee87435155d431
Quellennotizuspto-grants-2015_03