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HRID 727261作成日:2026年10月25日

Methylamine → HCID 68971298、化合物

https://huagongshe.com/reaction/727261

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
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 68971298HCID 68971298—

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 methylamine (0.69 g) in dimethylformamide (5 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 recrystallized from water/methanol to give 2.29 g of (S)-N-methyl-4-(4-chloro-phenyl)-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 143°-145° 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-a9af79cf68fe44bd955b58f6d97777a8
出典メモuspto-grants-1998_01