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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361446Generated: October 30, 2026

p-Toluenesulfonic acid monohydrate → 5-Methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine p-toluenesulfonic acid salt

https://huagongshe.com/reaction/1361446

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant5-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridineHCID 11186440—
SolventIsopropanolHCID 3776—
Product5-Methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine p-toluenesulfonic acid saltHCID 1118643990.5%

Reaction Steps

5-Methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine (1.00 g) was dissolved in 2-propanol (10 mL) at room temperature, and p-toluenesulfonic acid monohydrate (1.23 g) was added thereto at room temperature, followed by stirring at room temperature for 20 minutes. When the resultant mixture was cooled to 0° C., a salt was crystallized out of the mixture. After the resultant mixture was stirred at 0° C. for 2 hours, the precipitated salt was collected by filtration, and was washed with 2-propanol (2 mmol). The wet material was dried at room temperature under reduced pressure, to thereby give 1.91 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880005B2
Source datasetuspto-grants-2011_02
ORD IDord-a9fe379da6ca4b219e5e5fffac3c4f88
Source noteuspto-grants-2011_02