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HRID 236178作成日:2026年10月24日

Isopropanol → 2,3-Dihydro-4-methyl-2-[2-(4-morpholinyl)ethyl]-pyrido[3,2-f][1,4]oxazepin-5(4H)-one maleate

https://huagongshe.com/ja/reaction/236178

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物MorpholineHCID 8083—
反応物Sodium HydroxideHCID 14798—
反応物Maleic AcidHCID 444266—
反応物2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)one hydrochlorideHCID 13726437—
生成物2,3-Dihydro-4-methyl-2-[2-(4-morpholinyl)ethyl]-pyrido[3,2-f][1,4]oxazepin-5(4H)-one maleateHCID 13726489—

反応手順

2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)-one hydrochloride, 16 g (058 mole) was dissolved in morpholine (30 ml) and stirred overnight at room temperature. To the solution was added dilute sodium hydroxide solution (50 ml) and the resulting mixture extracted with chloroform (3×30 ml). The chloroform was removed on the rotary evaporator with aspiration. The residual morpholine was removed in vacuo at 50° C. (rotary evaporator). To the residual free base (15.5 g, 0.053 mole) was added isopropyl alcohol (1 liter) and maleic acid (9.24 g g, 0.080 mole). The mixture was heated to boiling and the clear solution cooled at 20° C. for several hours. The resulting crystals, 16 g (68.1%), were recrystallized from isopropyl alcohol, m.p. 163°-165° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04642343
出典データセットuspto-grants-1987_02
ORD IDord-49ae6b7c663b42968c086d3582186c6b
出典メモuspto-grants-1987_02