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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582386Generated: November 1, 2026

Sodium Hydroxide → N-(2-amidino-1,2,3,4-tetrahydro-5-isoquinolyl)methanesulfonamide

https://huagongshe.com/reaction/1582386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Methyl-2-thiopseudourea sulfateHCID 75270—
ReactantN-(1,2,3,4-tetrahydroisoquinolin-5-yl)methanesulfonamide hydrochlorideHCID 22218092—
SolventWaterHCID 962—
ProductN-(2-amidino-1,2,3,4-tetrahydro-5-isoquinolyl)methanesulfonamideHCID 1136919789%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred suspension of N-(1,2,3,4-tetrahydro-5-isoquinolyl)methanesulfonamide hydrochloride prepared as described in Example 19(b) of WO 98/30560 (100 g, 0.38 mol) and 2-methyl-2-thiopseudourea sulfate (159 g, 0.57 mol) in water (1.5 liter) was added 2N aqueous sodium hydroxide (764 ml, 1.53 mol). The resulting solution was warmed to 80° C. and stirred at this temperature for 6 hours and then left to cool to room temperature overnight. Further 2-methyl-2-thiopseudourea sulfate (27 g, 0.10 mol) and 2N aq. sodium hydroxide (48 ml, 0.10 mol) were charged and the mixture heated at 80° C. for 1 hour. After this time the resulting suspension was cooled to room temperature, filtered, washed with water (1 liter) to give a white solid that was dried in vacuo overnight at 50° C. to give 91.0 g of the title product (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734303B2
Source datasetuspto-grants-2004_05
ORD IDord-3a9383cd42db4fbd9500fa28d9ebf5cb
Source noteuspto-grants-2004_05