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HRID 616658作成日:2026年10月25日

Alprazolam → U 43465F

https://huagongshe.com/reaction/616658

反応式

関与物質

役割名称HCID仕込み量
反応物AlprazolamHCID 2118—
反応物N,N,N',N'-TetramethylmethanediamineHCID 5829—
反応物p-Toluenesulfonic acidHCID 6101—
反応物Acetyl chlorideHCID 6367—
反応物Sodium BicarbonateHCID 516892—
溶媒EthanolHCID 702—
溶媒DimethylformamideHCID 6228—
生成物U 43465FHCID 13438864.6%

反応手順

A stirred solution of N,N,N',N'-tetramethyldiaminomethane (2.244 g., 0.022 mole) in dry dimethylformamide (50 ml.) was cooled in an ice bath and treated dropwise with acetyl chloride (1.65 ml., 0.023 mole). The ice bath was removed and the mixture was kept at 25° for 45 min. and treated with 8-chloro-1-methyl-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine (3.09 g., 0.01 mole). After 30 min. the mixture was poured into ice water, made alkaline with sodium bicarbonate, saturated with sodium chloride and extracted with chloroform. The extract was washed with a dilute salt solution, dried over anhydrous sodium sulfate and concentrated in vacuo using xylene and toluene to help remove residual dimethylformamide. A solution of the residue in ethanol was acidified with a solution of one equivalent of p-toluenesulfonic acid in ethanol and crystallized to give 8-chloro-1-[2-(dimethylamino)ethyl]-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine p-toluenesulfonate in three crops; 2.69 g. of melting point 195°-196° C.; 0.751 g. of melting point 192°-195.5° C. and 0.033 g. of melting point 195°-197° C. The total yield was 64.6%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04075221
出典データセットuspto-grants-1978_02
ORD IDord-ea8ae3a6a41b4f1e826b97805378de71
出典メモuspto-grants-1978_02