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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1079907Erstellt: 25. Oktober 2026

Dimethylformamide → Desfluoro Iloperidone (Impurity)

https://huagongshe.com/reaction/1079907

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt4-(3-Chloropropoxy)-3-methoxyacetophenoneHCID 7314264—
Edukt3-(4-Piperidinyl)-1,2-benzisoxazole HydrochlorideHCID 13076437—
LösungsmittelWaterHCID 962—
ProduktDesfluoro Iloperidone (Impurity)HCID 1002442347,7%

Reaktionsschritte

A mixture of 3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (4.8 g, 20 mmol), K2CO3 (5.2 g, 40 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (5.3 g, 22 mmol), a few crystals of KI and dimethylformamide (60 ml) was stirred at 90 C. for 16 hours. The reaction was poured into water and the aqueous mixture was extracted with ethyl acetate. The extract was washed (water), dried (MgSO4) and concentrated to afford a brown oil. The oil was chromatographed on a Waters Prep 500 utilizing silica gel columns and ethyl acetate-diethylamine (2%), as eluent. Concentration of the appropriate fractions afforded 3.9 g of product as an off-white solid. Recrystallization from absolute ethyl alcohol afforded 2.6 g (33%) of 1-[4-[3-[4-(1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxypehenyl]ethanone, m.p.=102°-104° C., as colorless needles.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05580890
Quelldatensatzuspto-grants-1996_12
ORD IDord-f3f51ac021624790a4fc48a80909b7b1
Quellennotizuspto-grants-1996_12