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HRID 548783作成日:2026年10月25日

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

https://huagongshe.com/reaction/548783

反応式

関与物質

役割名称HCID仕込み量
反応物Trichloroisocyanuric AcidHCID 6909—
反応物IsopropylethanediolHCID 7996—
反応物5-Aminoimidazole-4-carboxamide hydrochlorideHCID 66146—
触媒TempoHCID 2724126—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物4-[(2-isopropoxyethyl)amino]-1H-imidazole-5-carboxamideHCID 6715755838.3%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943625B2
出典データセットuspto-grants-2011_05
ORD IDord-6673139033054c94a3ee28934054b163
出典メモuspto-grants-2011_05