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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616658생성일: 2026년 10월 25일

Alprazolam → U 43465F

https://huagongshe.com/reaction/616658

반응식

참여 물질

역할이름HCID투입량
반응물AlprazolamHCID 2118—
반응물N,N,N',N'-TetramethylmethanediamineHCID 5829—
반응물p-Toluenesulfonic acidHCID 6101—
반응물Acetyl chlorideHCID 6367—
반응물Sodium BicarbonateHCID 516892—
용매EthanolHCID 702—
용매DimethylformamideHCID 6228—
생성물U 43465FHCID 13438864.6%

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04075221
출처 데이터셋uspto-grants-1978_02
ORD IDord-ea8ae3a6a41b4f1e826b97805378de71
출처 메모uspto-grants-1978_02