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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46678생성일: 2026년 10월 24일

Hydrochloric Acid → Ticlopidine Hydrochloride

https://huagongshe.com/ko/reaction/46678

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Methanesulfonic AcidHCID 6395—
반응물Sodium HydroxideHCID 14798—
반응물N-((2-chlorophenyl)methyl)thiophene-3-ethylamineHCID 6454012—
용매EthanolHCID 702—
용매DimethylformamideHCID 6228—
생성물Ticlopidine HydrochlorideHCID 65335146.4%

반응 조건

온도20 °C

반응 단계

To 2.25 g (0.075 M) paraformaldehyde suspended in 20 ml dimethylformamide are added 9.61 g (0.1 M) methanesulfonic acid. The medium being at a temperature of 72° C., 13 g (0.05 M) N-(2-chloro-benzyl)-2-(2-thienyl)ethylamine dissolved in 5 ml dimethylformamide are added over 2 minutes. The temperature of the reaction medium reaches 90° C. The reaction medium is then cooled to 20° C. and poured over 50 ml 4N sodium hydroxide. The material is extracted with 1×30 ml and then 1×20 ml methylene chloride. The organic phases are combined, dried over sodium sulfate and evaporated, to give an oil which is taken up into 30 ml ethanol in which are dissolved 0.15 mole gaseous hydrochloric acid. After partial evaporation of the ethanol, the desired product precipitates out. It is filtered, washed with acetone and dried, to give 11.35 g 5-(2-chloro-benzyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (Yield: 75.6%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04174448
출처 데이터셋uspto-grants-1979_11
ORD IDord-6a087057b35f4230abd8f03b91abb4e0
출처 메모uspto-grants-1979_11