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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2178609Erstellt: 24. Oktober 2026

Acetic Acid → USRE48711, Example 234

https://huagongshe.com/de/reaction/2178609

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2-Propanamine, 1-methoxy-, (2S)-HCID 7021536—
EduktN,N-dimethylformamide N,N-dimethylacetamideHCID 22628260—
Edukt6-cyclopropyl-N-(6-(hydrazinecarbonyl)pyridin-2-yl)-3,4'-bipyridine-2'-carboxamideHCID 58103016—
LösungsmittelTolueneHCID 1140—
ProduktUSRE48711, Example 234HCID 6685173063%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

To a suspension of 6-cyclopropyl-N-(6-(hydrazinecarbonyl)pyridin-2-yl)-3,4′-bipyridine-2′-carboxamide, a compound of formula (3) (75 mg, 0.20 mmol) in toluene (0.20 M) was added N,N-dimethylformamide/N,N-dimethylacetamide (67 μL, 0.50 mmol), (S)-2-methoxy-1-methyl-ethylamine (72 mg μL, 0.80 mmol), and acetic acid (11 μL, 0.20 mmol). The reaction was heated to 150° C. for 30 minutes in a microwave reactor. The reaction mixture was concentrated under reduced pressure, and the residue suspended in acetonitrile/diethyl ether (15 mL, 1:1 ratio), filtered and washed with acetonitrile/diethyl ether (2×10 mL). The solid thus obtained was dried under reduced pressure to afford 57 mg (63% yield) of (S)-6-cyclopropyl-N-(6-(4-(1-methoxypropan-2-yl)-4H-1,2,4-triazol-3-yl)pyridin-2-yl)-3,4′-bipyridine-2′-carboxamide as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09067933B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-6ffcc631fe4646d2b76fa03abc6fa119
Quellennotizuspto-grants-2015_06