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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2234643Erstellt: 25. Oktober 2026

Diisopropylethylamine → 1-(2,2,2-trifluoro-acetyl)-pyrrolidine-2-carboxylic Acid {2-dimethylcarbamoyl-6-fluoro-4-[3-(2-methoxy-phenyl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-phenyl}-amide

https://huagongshe.com/reaction/2234643

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktN-Trifluoroacetylprolyl chlorideHCID 3082449—
Edukt2-amino-3-fluoro-5-[3-(2-methoxy-phenyl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-N,N-dimethyl-benzamideHCID 57731478—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(2,2,2-trifluoro-acetyl)-pyrrolidine-2-carboxylic Acid {2-dimethylcarbamoyl-6-fluoro-4-[3-(2-methoxy-phenyl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-phenyl}-amideHCID 86630892—

Reaktionsschritte

To a scintillation vial was combined 32 mg (0.06 mmol) of 2-amino-3-fluoro-5-[3-(2-methoxy-phenyl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-N,N-dimethyl-benzamide and 15 uL (0.09 mmol) of N,N-diisopropylethylamine. To the vial was added 745 μL of a 0.1M solution of (S)-(−)-N-(trifluoroacetyl)prolylchloride in dichloromethane. The reaction was stirred at room temperature for 30 minutes, quenched with a few drops of methanol, and concentrated down. MS: m/z 752.1 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07709645B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-915d43fe1b034e1ab93b29ec3ae69851
Quellennotizuspto-grants-2010_05