돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548783생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Trichloroisocyanuric AcidHCID 6909—
반응물IsopropylethanediolHCID 7996—
반응물5-Aminoimidazole-4-carboxamide hydrochlorideHCID 66146—
촉매TempoHCID 2724126—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물4-[(2-isopropoxyethyl)amino]-1H-imidazole-5-carboxamideHCID 6715755838.3%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07943625B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-6673139033054c94a3ee28934054b163
출처 메모uspto-grants-2011_05