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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46678Generated: October 26, 2026

Hydrochloric Acid → Ticlopidine Hydrochloride

https://huagongshe.com/reaction/46678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
ReactantN-((2-chlorophenyl)methyl)thiophene-3-ethylamineHCID 6454012—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductTiclopidine HydrochlorideHCID 65335146.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174448
Source datasetuspto-grants-1979_11
ORD IDord-6a087057b35f4230abd8f03b91abb4e0
Source noteuspto-grants-1979_11