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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1828272Erstellt: 26. Oktober 2026

Diisopropylethylamine → 2-[4-(1-Benzothien-2-ylmethyl)-1-piperazinyl]benzonitrile

https://huagongshe.com/reaction/1828272

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktMethanesulfonic anhydrideHCID 81560—
EduktN-(2-Cyanophenyl)piperazineHCID 2735875—
Edukt2-(Hydroxymethyl)benzo[b]thiopheneHCID 2776335—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-[4-(1-Benzothien-2-ylmethyl)-1-piperazinyl]benzonitrileHCID 9996948—

Reaktionsschritte

The product from Example 8A (150 mg 0.9 mmol), methane sulfonic anhydride (159 mg, 0.9 mmol), and DIEA (475 μL 2.7 mmol) were combined. After stirring, 2-(1-piperazinyl)benzonitrile (181 mg, 1.0 mmol) in 2 ml DCM was also combined and stirred at room temperature for 18 hours. The mixture was concentrated and the residue was taken up in hot methanol. The methanol was filtered and the filter cake washed with cold methanol to provide the title compound. 1H NMR (300 MHz, CDCl3) δ 2.69 (m, 4H) 3.04 (s, 4H) 3.76 (m, 4H) 3.86 (s, 1H) 6.74 (m, 2H) 7.29 (m, 3H) 7.75 (m, 1H); (ESI) m/z 334 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07057042B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-ff2ec1e989874245ab56f51bea23a15c
Quellennotizuspto-grants-2006_06