Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetate | HCID 175 | — |
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | 2-Methoxybenzylamine | HCID 81292 | — |
| Edukt | 1-(2-Pyridyl)-2-thiourea | HCID 1490491 | — |
| Edukt | HCID 178489506 | HCID 178489506 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 178476648 | HCID 178476648 | — |
Reaktionsschritte
0.800 g (5.117 mmol) N-pyridin-2-yl-thiourea was dissolved in 10 mL methanol, 0.45 mL (7.164 mmol) methyl iodide in 5 mL methanol was added dropwise, and the mixture was heated for 1 hr at 70° C. (oil bath temperature) and subsequently stirred at room temperature. The solvent was removed under vacuum and the intermediate product, methyl N-(pyridin-2-yl)imidothiocarbamate hydroiodide, was redissolved in 15 mL ethanol. 1.36 mL (10.235 mmol) 2-methoxybenzylamine was added dropwise, and the mixture was heated for 2.75 hr at 85° C. (oil bath temperature) and subsequently stirred at room temperature. The solvent was then evaporated under vacuum. The crude product was redissolved with dichloromethane and extracted with water (2×30 mL). After drying over magnesium sulfate and removal of the solvent, purification was carried out via preparative HPLC (Merck Chromolith RP-18 100×25 mm, eluent: water/acetonitrile/0.1 M acetic acid). For complete ion exchange with the ion exchanger (Fluka, acetate on 1.5 mmol CH3COO/g/resign polymer substrate), the purified N-(2-methoxybenzyl)-N′-pyridin-2-yl-guanidine was converted to the acetate salt in a yield of 0.357 g (1.128 mmol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09296697B2 |
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| Quelldatensatz | uspto-grants-2016_03 |
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| ORD ID | ord-4dab30cdce564b958260e3aef1a44e3b |
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| Quellennotiz | uspto-grants-2016_03 |
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