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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2216063Erstellt: 25. Oktober 2026

Ethanol → tert-butyl N-[4-[3-(3-amino-5-methyl-4-pyridinyl)phenyl]sulfonyl-5-methylsulfanylthiophene-2-carboximidoyl]carbamate

https://huagongshe.com/reaction/2216063

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktTolueneHCID 1140—
Edukt(4-Iodo-5-methyl-pyridin-3-yl)-carbamic acid tert-butyl esterHCID 60026355—
EduktHCID 178419158HCID 178419158—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium CarbonateHCID 10340—
Produkttert-butyl N-[4-[3-(3-amino-5-methyl-4-pyridinyl)phenyl]sulfonyl-5-methylsulfanylthiophene-2-carboximidoyl]carbamateHCID 145857697—

Reaktionsschritte

(4-Iodo-5-methyl-pyridin-3-yl)-carbamic acid tert-butyl ester (106 mg, 0.32 mmol, Example 139: step b), {[4-(3-Boranyl-dihydroxy-benzenesulfonyl)-5-methylsulfanyl-thiophen-2-yl]-imino-methyl}-carbamic acid tert-butyl ester (145 mg, 0.32 mmol, Example 140: step a) and Pd(PPh3)4 (74 mg, 0.06 mmol) were combined in aqueous Na2CO3 (2M, 1.2 mL), ethanol (1.2 mL) and toluene (2.4 mL) and was heated to 80° C. overnight. The reaction mixture was dissolved into EtOAc and washed with brine. The organic layers were dried (MgSO4) and solvents were removed in vacuo. Purification by flash column chromatography (40% EtOAc/hexanes) afforded the title compound. ESI-MS (m/z): Calcd. for C28H34N4O6S3: 619.2 (M+1); found: 618.8.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07109354B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-bdac16c0a6e84c5b98a1a9d6d963f622
Quellennotizuspto-grants-2006_09