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HRID 2422704Erstellt: 26. Oktober 2026

Pyridine → (R,R)-N-[3-(4-hydroxyphenyl)-4-methylisothiazol-5-yl]-2-methylcyclopropanecarboxamide

https://huagongshe.com/reaction/2422704

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDichloromethaneHCID 6344—
EduktOxalyl chlorideHCID 65578—
Eduktrel-(1R,2R)-2-Methylcyclopropanecarboxylic acidHCID 6995705—
Edukt4-(5-Amino-4-methylisothiazol-3-yl)phenolHCID 136355285—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(R,R)-N-[3-(4-hydroxyphenyl)-4-methylisothiazol-5-yl]-2-methylcyclopropanecarboxamideHCID 13624423764,6%

Reaktionsschritte

Add oxalyl chloride (2 M in dichloromethane, (0.291 mL, 0.583 mmol) to a stirred solution of (R,R)-2-methylcyclopropanecarboxylic acid (0.06 g, 0.58 mmol) and DMF (1 drop-catalytic) in toluene (1 mL). Stir 3 h and add the now formed acid chloride to a stirred solution of 4-(5-amino-4-methylisothiazol-3-yl)phenol (0.060 g, 0.291 mmol) and pyridine (0.07 g, 0.87 mmol) in THF (1 mL). Stir 1 h and dilute with EtOAc (300 mL), and wash with 1 N NaOH (2 times 100 mL) then water (100 mL), dry (MgSO4) and evaporate. Crystallize from chloroform and hexane. Yield: 64.6%. ES-MS: m/e 289.0 (m+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07960419B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-ad34b95702754957aa30c7779bafce6d
Quellennotizuspto-grants-2011_06