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HRID 1186558Erstellt: 25. Oktober 2026

N-methylthiophen-3-amine → HCID 68226672, Verbindung

https://huagongshe.com/reaction/1186558

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-methylthiophen-3-amineHCID 642344—
Edukt2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
EduktSodium t-butoxideHCID 23676156—
EduktHCID 86670921HCID 86670921—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 68226672HCID 68226672—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of {4-[3-(6-bromo-pyridin-2-yl)-imidazo[1,2-a]pyrazin-8-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester (from Example 40 supra) (0.244 g, 0.5 mmol), compound thiophen-3-yl-methylamine (0.113 g, 1.0 mmol), Pd2(dba)3 (30 mg), Davephos (40 mg), NaOtBu (100 mg, 0.1 mmol) in dioxane (12 mL) in a sealed tube was bubbled with N2 for several minutes and then heated under N2 at 110° C. for 16 hours. The solution was then cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by chromatography (CH2Cl2:MeOH, 100:1) to give [4-(3-{6-[(thiophen-3-ylmethyl)-amino]-pyridin-2-yl}-imidazo[1,2-a]pyrazin-8-ylamino)-cyclohexyl]-carbamic acid tert-butyl ester. (Yield 70 mg, 27%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08673905B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-3b9205c5487847f39e70bb464ea00fc6
Quellennotizuspto-grants-2014_03