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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13342Erstellt: 25. Oktober 2026

Water → t-Butyl 2-(4-amino-2-(4-methanesulfonyl-phenoxy)-5-nitro-phenyl)-pyrrole-1-carboxylate

https://huagongshe.com/reaction/13342

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
Edukt1-(tert-Butoxycarbonyl)-2-pyrroleboronic AcidHCID 2734321—
Edukt4-Bromo-5-(4-methanesulfonyl-phenoxy)-2-nitro-phenylamineHCID 23145228—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produktt-Butyl 2-(4-amino-2-(4-methanesulfonyl-phenoxy)-5-nitro-phenyl)-pyrrole-1-carboxylateHCID 23145143—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

7.9 g of 1-(t-butoxycarbonyl)pyrrole-2-boronic acid, 1.8 g of dichlorobistriphenylphosphine palladium, 50 ml of aqueous saturated sodium carbonate solution and 50 ml of water were added in order to a dimethoxyethane (100 ml) solution of 10.3 g of 4-bromo-5-(4-methanesulfonyl-phenoxy)-2-nitro-phenylamine, and the reaction liquid was stirred in a nitrogen atmosphere at 80° C. for 1 hour. After cooled, the reaction liquid was filtered through Celite, the filtrate was diluted with ethyl acetate, washed with water and saturated saline in order, and then dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=1/1) to obtain the entitled compound as a brown oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728025B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-84d1dd9f7dda4836b1bb8da6482e292d
Quellennotizuspto-grants-2010_06