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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 929654Erstellt: 25. Oktober 2026

Acetate → HCID 178476648, Verbindung

https://huagongshe.com/reaction/929654

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetateHCID 175—
EduktMethyl iodideHCID 6328—
Edukt2-MethoxybenzylamineHCID 81292—
Edukt1-(2-Pyridyl)-2-thioureaHCID 1490491—
EduktHCID 178489506HCID 178489506—
LösungsmittelMethanolHCID 887—
ProduktHCID 178476648HCID 178476648—

Reaktionsbedingungen

Temperatur70 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09296697B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-4dab30cdce564b958260e3aef1a44e3b
Quellennotizuspto-grants-2016_03