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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2427720Erstellt: 26. Oktober 2026

Mechlorethamine → 7-Methyl-5-(4-methyl-piperazin-1-ylmethyl)-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one

https://huagongshe.com/reaction/2427720

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMechlorethamineHCID 4033—
EduktPotassium CarbonateHCID 11430—
Edukt5-Aminomethyl-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-oneHCID 57949320—
LösungsmittelDimethylformamideHCID 6228—
Produkt7-Methyl-5-(4-methyl-piperazin-1-ylmethyl)-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-oneHCID 5794940631%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

In sealed vial, a mixture of 5-aminomethyl-7-methyl-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.104 g, 0.3 mmol), bis(2-chloro-ethyl)-methyl-amine (0.077 g, 0.4 mmol), and K2CO3 (0.083 g, 0.6 mmol) in DMF (3 mL) was stirred at 110° C. for 16 h. After this time, the GC-MS of the reaction mixture indicated the completion of reaction. The reaction was cooled to ambient temperature and the solids removed by filtration. The filtrate was concentrated. Silica gel column chromatography of the resulting material using 5:1 CHCl3-MeOH afforded 7-methyl-5-(4-methyl-piperazin-1-ylmethyl)-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.040 g, 31%). 1H NMR (300 MHz, CDCl3): δ (ppm) 2.24 (s, 3H), 2.34-2.52 (m, 8H), 2.74 (s, 3H), 3.49 (s, 2H), 4.20 (s, 2H), 4.76 (s, 2H), 7.15-7.37 (m, 6H). GC-MS: m/z 433 (M)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07968570B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-d6fdfeea6ef14a189a92dc3c871e7335
Quellennotizuspto-grants-2011_06