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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1792906Erstellt: 25. Oktober 2026

Carbamimidoylazanium Chloride → HCID 178462846, Verbindung

https://huagongshe.com/reaction/1792906

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbamimidoylazanium ChlorideHCID 5460839—
EduktPotassium tert-butoxideHCID 23665647—
Eduktethyl (2-ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetateHCID 86591360—
LösungsmittelWaterHCID 962—
ProduktHCID 178462846HCID 17846284628%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

N-[(2-Ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetyl]guanidine is prepared as described in Example 1, starting with 4.3 g of potassium tert-butoxide, 3.7 g of guanidinium chloride and 1.9 g of ethyl (2-ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetate. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours, followed by addition of 60 cm3 of water. The aqueous phase is extracted with 3 times 50 cm3 of ethyl acetate and is then concentrated to dryness under reduced pressure (0.6 kPa) at a temperature in the region of 45° C. The residue is taken up in water, triturated and filtered. The solid is taken up in methanol and the solvent is then evaporated to dryness under reduced pressure (0.6 kPa) at a temperature in the region of 45° C. 0.56 g of N-[(2-ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetyl]-guanidine is thus obtained in the form of an off-white solid melting at 223° C. Mass spectrum EI: m/e 260 (M+), m/e 173, m/e 160, m/e 132.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07078428B2
Quelldatensatzuspto-grants-2006_07
ORD IDord-3070f13bd72545d38a8514b0b4057615
Quellennotizuspto-grants-2006_07