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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1408430Erstellt: 25. Oktober 2026

Potassium Carbonate → methyl 6-[3-[4-chloro-3-[[(methoxycarbonyl)amino]-methyl]phenyl]-1H-pyrazol-1-yl]-2H-1-benzopyran-3-carboxylate

https://huagongshe.com/reaction/1408430

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
EduktMethyl 6-bromo-2H-1-benzopyran-3-carboxylateHCID 15272849—
EduktHCID 178502067HCID 178502067—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Lösungsmittel1,4-DioxaneHCID 31275—
LösungsmittelChloroform methanolHCID 21584188—
Produktmethyl 6-[3-[4-chloro-3-[[(methoxycarbonyl)amino]-methyl]phenyl]-1H-pyrazol-1-yl]-2H-1-benzopyran-3-carboxylateHCID 6715115316%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of methyl N-[[2-chloro-5-(1H-pyrazol-3-yl)phenyl]-methyl]carbamate (i.e. the product of Step B) (400 mg, 1.50 mmol) in dioxane (16 mL) was added trans-N,N′-dimethylcyclohexane-1,2-diamine (0.30 mmol, 43 mg) under a nitrogen atmosphere. Copper (I) iodide (57 mg, 0.30 mmol) and K2CO3 (1.24 g, 9.05 mmol) were added to the reaction mixture. Methyl 6-bromo-2H-1-benzopyran-3-carboxylate (607 mg, 2.26 mmol) was added to the reaction mixture last. The reaction mixture was heated at 100° C. under a nitrogen atmosphere overnight. After TLC analysis (10% MeOH/CHCl3) showed 80% conversion of the starting material, the reaction mixture was cooled and concentrated under vacuum. The crude residue was purified on a silica gel column with 1% MeOH/CHCl3 as eluent to give compound number 23, a compound of the present invention, (110 mg, 16% yield) as solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08921360B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-42f5735f75894aea86911a143536fa42
Quellennotizuspto-grants-2014_12