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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Methyl-2-thiopseudourea sulfate | HCID 75270 | — |
| Reactant | N-(1,2,3,4-tetrahydroisoquinolin-5-yl)methanesulfonamide hydrochloride | HCID 22218092 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-amidino-1,2,3,4-tetrahydro-5-isoquinolyl)methanesulfonamide | HCID 11369197 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06734303B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-3a9383cd42db4fbd9500fa28d9ebf5cb |
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| Source note | uspto-grants-2004_05 |
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