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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245744Erstellt: 25. Oktober 2026

1H-Indole-2-carboxylic acid, 1-methyl- → HCID 178432917, Verbindung

https://huagongshe.com/reaction/245744

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1H-Indole-2-carboxylic acid, 1-methyl-HCID 27695—
Edukt4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
Edukt1-methyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-indole-2-carboxamideHCID 18450543—
EduktHCID 178432912HCID 178432912—
ProduktHCID 178432917HCID 17843291727,9%

Reaktionsschritte

Reaction of 1-methyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-indole-2-carboxamide (29 mg), prepared from 1-methyl-1H-indole-2-carboxylic acid which was transformed into its acid chloride first and then reacted with 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, and 1-bromo-8-methyl-3-((trans)-4-(4-methylpiperazin-1-yl)cyclohexyl)imidazo[1,5-a]pyrazine (30 mg) according to the procedure described in example 4 step 4c and purification by column chromatography (silica gel; dichloromethane with gradient 0 to 20% of methanol) gave 1-methyl-N-(4-(8-methyl-3-((trans)-4-(4-methylpiperazin-1-yl)cyclohexyl)imidazo[1,5-a]pyrazin-1-yl)phenyl)-1H-indole-2-carboxamide (12 mg)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658794B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-448dea8b6c55473c849f56cd0dd53cd5
Quellennotizuspto-grants-2014_02