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HRID 727262作成日:2026年10月24日

Ethanolamine → HCID 68973505、化合物

https://huagongshe.com/reaction/727262

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
反応物TriethylamineHCID 8471—
反応物Pivaloyl chlorideHCID 62493—
反応物2-((9S)-7-(4-chlorophenyl)-4,5,13-trimethyl-3-thia-1,8,11,12-tetraazatricyclo(8.3.0.0,2,6)trideca-2(6),4,7,10,12-pentaen-9-yl)acetic acidHCID 66828107—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 68973505HCID 6897350529.5%

反応条件

温度-5 °C

反応手順

(S)-4-(4-Chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f]-[1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid (7.0 g) and triethylamine (2.73 ml) are added to a mixed solvent of dimethylformamide (70 ml) and tetrahydrofuran (30 ml). The mixture is cooled to -5° C., and pivaloyl chloride (2.38 ml) is dropwise added at said temperature. Ten minutes later, a solution of ethanolamine (1.17 g) in tetrahydrofuran (10 ml) is dropwise added at said temperature, and the mixture is stirred at room temperature for 2 hours. Water is added to the reaction mixture, and the mixture is extracted with ethyl acetate, washed with water and dried over anhydrous magnesium sulfate. The solvent is distilled away, and the residue is purified by column chromatography (chloroform: methanol =50: 1) and recrystallized from ethyl acetate to give 2.29 g of (S)-N-(2-hydroxyethyl)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetamide 1/4 hydrate, melting point 254°-255° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05712274
出典データセットuspto-grants-1998_01
ORD IDord-58e0de326b254e8f9ed58e5d6aa2dedb
出典メモuspto-grants-1998_01