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HRID 981459作成日:2026年10月26日

Etizolam → ethyl 6-amino-4-(2-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]-triazolo[4,3-a][1,4]diazepine-6-carboxylate

https://huagongshe.com/reaction/981459

反応式

関与物質

役割名称HCID仕込み量
反応物EtizolamHCID 3307—
反応物Diethyl CarbonateHCID 7766—
反応物Sodium hydrideHCID 24758—
反応物O-(2,4-dinitrophenyl)hydroxylamineHCID 87140—
反応物HCID 178418361HCID 178418361—
溶媒Acetic AcidHCID 176—
生成物ethyl 6-amino-4-(2-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]-triazolo[4,3-a][1,4]diazepine-6-carboxylateHCID 15662236—

反応条件

温度20 °C

反応手順

To 500 ml of diethyl carbonate were added 22.0 g of 4-(2-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]-triazolo[4,3-a][1,4]diazepine and 4.3 g of sodium hydride, and the mixture was heated. Hydrogen gas began to generate at about 100° C., while the solution gradually colored violet. After 30 minutes' reflux, the mixture was cooled to 20° C., whereto 16.0 g of O-(2,4-dinitrophenyl)hydroxylamine was added. The mixture was stirred for 2 hours. After the completion of the reaction, the reaction mixture was poured into ice-water containing 6 ml of acetic acid. The diethyl carbonate layer was separated, washed twice with water and dried over anhydrous magnesium sulfate. Diethyl carbonate was distilled off under reduced pressure, and diisopropyl ether was added to the obtained residue to separate crystals, which were collected by filtration. The crystals were recrystallized from ethyl acetate to give 18.2 g of ethyl 6-amino-4-(2-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]-triazolo[4,3-a][1,4]diazepine-6-carboxylate, m.p. 180°-181° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04992437
出典データセットuspto-grants-1991_02
ORD IDord-9afa05ec484447ffa9964d40d620868f
出典メモuspto-grants-1991_02