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HRID 46678作成日:2026年10月25日

Hydrochloric Acid → Ticlopidine Hydrochloride

https://huagongshe.com/reaction/46678

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物FormaldehydeHCID 712—
反応物Methanesulfonic AcidHCID 6395—
反応物Sodium HydroxideHCID 14798—
反応物N-((2-chlorophenyl)methyl)thiophene-3-ethylamineHCID 6454012—
溶媒EthanolHCID 702—
溶媒DimethylformamideHCID 6228—
生成物Ticlopidine HydrochlorideHCID 65335146.4%

反応条件

温度20 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04174448
出典データセットuspto-grants-1979_11
ORD IDord-6a087057b35f4230abd8f03b91abb4e0
出典メモuspto-grants-1979_11