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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1768342Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1768342

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
PatentnummerUS07235661B2
Quelldatensatzuspto-grants-2007_06
ORD IDord-098f2f3cd58a4f809fca19fa91d79180
Quellennotizuspto-grants-2007_06