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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 548783Erstellt: 24. Oktober 2026

Trichloroisocyanuric Acid → 4-[(2-isopropoxyethyl)amino]-1H-imidazole-5-carboxamide

https://huagongshe.com/de/reaction/548783

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrichloroisocyanuric AcidHCID 6909—
EduktIsopropylethanediolHCID 7996—
Edukt5-Aminoimidazole-4-carboxamide hydrochlorideHCID 66146—
KatalysatorTempoHCID 2724126—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[(2-isopropoxyethyl)amino]-1H-imidazole-5-carboxamideHCID 6715755838,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Trichlorocyanuric acid (1.23 g, 5.29 mmol) was added to a solution of 2-isopropoxyethanol (0.50 g, 4.80 mmol) in CH2Cl2 (3 mL). The reaction mixture was cooled to 0° C. and TEMPO (0.015 g, 0.09 mmol) was carefully added in small portions. The mixture was stirred at r.t. for 20 minutes and then filtrated through Celite and washed with CH2Cl2. The filtrate was kept cold, 0° C., during the filtration. The obtained aldehyde solution was added to a stirred mixture of 4-amino-1H-imidazole-5-carboxamide hydrochloride (0.78 g, 4.80 mmol), which was obtained from Example 3(b), at 0° C. in MeOH (5 mL). The mixture was stirred for 20 minutes, then NaCNBH4 (0.30 g, 4.80 mmol) was added. After stirring at r.t for 5 h the mixture was concentrated and purified by flash chromatography (CH2Cl2/methanol gradient; 0 to 5% methanol), to yield the title compound (0.39 g, 38%) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943625B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-6673139033054c94a3ee28934054b163
Quellennotizuspto-grants-2011_05