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HRID 35640作成日:2026年10月23日

Diketene → N-Methyl-N-[3-(3-methyl-1,2,4-triazolo-[4,3-b]-pyridazin-6-yl)phenyl]-3-oxo-butanamide

https://huagongshe.com/ja/reaction/35640

反応式

関与物質

役割名称HCID仕込み量
反応物DiketeneHCID 12661—
反応物N-Methyl-3-(3-Methyl[1,2,4]Triazolo[4,3-B]Pyridazin-6-Yl)AnilineHCID 2779723—
溶媒TolueneHCID 1140—
生成物N-Methyl-N-[3-(3-methyl-1,2,4-triazolo-[4,3-b]-pyridazin-6-yl)phenyl]-3-oxo-butanamideHCID 15595682—

反応手順

A mixture of 2.0 g of N-methyl-3-(3-methyl-1,2,4-triazolo-[4,3-b]pyridazin-6-yl)benzenamine and 2.14 ml of diketene in 250 ml of dry toluene was heated to reflux for 2 days. The solution was concentrated in vacuo and the residue partitioned between 300 ml dichloromethane and 200 ml of water. The aqueous layer was extracted with 150 ml portions of dichloromethane. The organic layer and extracts were combined, dried and concentrated in vacuo. The residue was chromatographed on 300 g of silica gel with dichloromethane-methanol (97:3). The fractions containing product were combined, evaporated in vacuo and the solid recrystalized from dichloromethane-hexane to give 1.15 g of tan crystals, mp 138°-141° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04767765
出典データセットuspto-grants-1988_08
ORD IDord-d6294640900645d18814bf4b5cb8d64f
出典メモuspto-grants-1988_08