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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 454330Erstellt: 24. Oktober 2026

Sulfuric Acid → HCID 178496565, Verbindung

https://huagongshe.com/de/reaction/454330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktTrifluoroacetic acidHCID 6422—
EduktSodium CarbonateHCID 10340—
EduktHCID 178496566HCID 178496566—
EduktHCID 178496567HCID 178496567—
ProduktHCID 178496565HCID 17849656567%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

5-(8-(((trans)-4-Methoxycyclohexyl)methyl)-7-oxo-5,6,7,8-tetrahydropyrazino[2,3-b]pyrazin-2-yl)-4-methylpicolinamide. 5-(8-(((trans)-4-Methoxycyclohexyl)methyl)-7-oxo-5,6,7,8-tetrahydropyrazino[2,3-b]pyrazin-2-yl)-4-methylpicolinonitrile (0.607 g, 1.55 mmol), trifluoroacetic acid (2.0 mL, 26.0 mmol) and sulfuric acid (0.5 mL, 9.38 mmol) were combined and heated at 65° C. for 1 h. Reaction pH was adjusted to 10 with sodium carbonate and the resulting solution was extracted with ethyl acetate (3×15 mL). Organic layers were collected, dried over magnesium sulfate, concentrated and purified using reverse-phase preparatory HPLC (10-100% acetonitrile+0.1% TFA in H2O+0.1% TFA, over 30 min). Clean fractions were combined and condensed under reduced pressure and dried under high vacuum to afford the title compound as a yellow solid (0.425 g, 1.04 mmol, 67% yield). MS (ESI) m/z 411.5 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08492381B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-de99d449512e43ebb4a87d30bb7cb399
Quellennotizuspto-grants-2013_07