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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13463Erstellt: 23. Oktober 2026

1-Pyrrolidineethanamine → 4-(2-{[2-fluro-5-(trifluromethyl)phenyl]amino-1-methylbenzimidazol-5-yloxy)-(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide

https://huagongshe.com/de/reaction/13463

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-PyrrolidineethanamineHCID 1344—
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Edukt2-{[2-Fluoro-5-(trifluoromethyl)phenylamino)-1-methylbenzimidazol-5-yl-oxy)pyridine-2-carboxylic acidHCID 86592199—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(2-{[2-fluro-5-(trifluromethyl)phenyl]amino-1-methylbenzimidazol-5-yloxy)-(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamideHCID 131725836—

Reaktionsschritte

To 4-(2-{[2-fluoro-5-(trifluoromethyl)phenylamino)-1-methylbenzimidazol-5-yloxy)pyridine-2-carboxylic acid (1 eq) in tetrahydrofuran was added 2-pyrrolidinylethylamine (2 eq), HBTU (2 eq) and N,N-diisopropylethylamine (4 eq) and stir at ambient temperature for 16 h. The mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was concentrated and preparative chromatography yielded [4-(2-{[2-fluoro-5-(trifluoromethyl)phenyl]amino-1-methylbenzimidazol-5-yloxy)-(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide. MS: MH+=542.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728010B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-df538d82fa4945c9b3edd0f86a5fd893
Quellennotizuspto-grants-2010_06