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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270704Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-Amino-2-(methylsulfanyl)pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/270704

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium CarbonateHCID 10340—
Edukt4-Amino-2-(methylsulfanyl)pyrimidine-5-carbonitrileHCID 295757—
EduktDiisobutylaluminumhydrideHCID 21225700—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Amino-2-(methylsulfanyl)pyrimidine-5-carbaldehydeHCID 29576953,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 4-amino-2-(methylthio)pyrimidine-5-carbonitrile (3.0 g, 18.05 mmol) in THF (100 mL) is added diisobutylaluminum hydride (41.52 mL, 1.0 M in CH2Cl2, 41.52 mmol) at 0° C. After the mixture is stirred for 2.5 hours at 0° C., hydrochloric acid (2N, 30 mL) is added and stirring is continued for 20 minutes. To the reaction mixture is added saturated Na2CO3 until a pH of 8 is achieved. The suspended material is filtered through Celit pad and washed with K2CO3 solution. The solution is diluted with EtOAc and washed with saturated K2CO3, brine and dried, filtered and concentrated to give crude product, which is purified by flash silica gel column, eluting with hexane (100%) gradient to hexane/ether (60/40%), to give the title intermediate as a solid (1.62 g, 53.1%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07449582B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-4f82a12b8b6b4e0b823e207cd72b0dda
Quellennotizuspto-grants-2008_11