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HRID 361323作成日:2026年10月27日

Boron trifluoride etherate → 10,11-dihydro-10-methoxycarbonylpropylimino-5H-dibenz[b,f]azepine-5-carboxamide

https://huagongshe.com/reaction/361323

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物OxcarbazepineHCID 34312—
反応物4-Aminobutyric acid methyl ester hydrochlorideHCID 2756383—
溶媒O-XyleneHCID 7237—
生成物10,11-dihydro-10-methoxycarbonylpropylimino-5H-dibenz[b,f]azepine-5-carboxamideHCID 57155718—

反応条件

温度135 °C

反応手順

To a suspension of 0.2 g (0.79 mmol) of 10,11-dihydro-10-oxo-5H-dibenz[b,f]azepine-5-carboxamide and 0.1 g (0.67 mmol) of methyl-4-aminobutyrate hydrochloride in 5 mL of xylene was added 0.07 g (0.49 mmol) of boron trifluoride diethyl etherate. The resulting mixture was heated at 135° C. for seven hours and then allowed to cool to room temperature. The mixture was then filtered and the residue was extracted with toluene. The combined extracts were evaporated under reduced pressure and the residue chromatographed on silica gel using a 4:1 mixture of petroleum ether-ethyl acetate. Chromatographically homogenous fractions were pooled and the solvents were removed under reduced pressure to give the desired product as a yellow oil which crystallised on standing to give yellow crystals which decomposed on heating without melting.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05866566
出典データセットuspto-grants-1999_02
ORD IDord-711b24ff6bee4af983e5f51cecb84810
出典メモuspto-grants-1999_02