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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 575269Erstellt: 25. Oktober 2026

10-bromo-3((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide → (R)-10-((3-hydroxy-1-methyl-2-oxopyrrolidin-3-yl)ethynyl)-3-((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide

https://huagongshe.com/reaction/575269

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt10-bromo-3((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamideHCID 86693288—
Edukt(R)-3-ethynyl-3-hydroxy-1-methylpyrrolidin-2-oneHCID 86693296—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt(R)-10-((3-hydroxy-1-methyl-2-oxopyrrolidin-3-yl)ethynyl)-3-((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamideHCID 8669329519%

Reaktionsschritte

Similar to as described in General Procedure E with the exceptions of using Pd(PPh3)4 in DMSO, 10-bromo-3-((2-methyl-1H-benzo[d]imidazol-1-yl)methyl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide was reacted with (R)-3-ethynyl-3-hydroxy-1-methylpyrrolidin-2-one to yield the titled compound as a yellow solid (21 mg, 19%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09034866B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-5196f80411df498c84b7d4b2984b16a9
Quellennotizuspto-grants-2015_05