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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 391015생성일: 2026년 10월 24일

Acetamidine monohydrochloride → 5-Bromo-2-methylpyrimidine-4-carboxylic acid

https://huagongshe.com/ko/reaction/391015

반응식

참여 물질

역할이름HCID투입량
반응물Acetamidine monohydrochlorideHCID 67170—
반응물Sodium ethoxideHCID 2723922—
반응물Mucobromic AcidHCID 3033972—
용매EthanolHCID 702—
생성물5-Bromo-2-methylpyrimidine-4-carboxylic acidHCID 25621025.4%

반응 조건

온도50 °C

반응 단계

To a solution of acetamidine hydrochloride (6.0 g) in ethanol (20 mL) was added sodium ethoxide (20 mL of a 21% solution in ethanol) and the reaction mixture was heated at 50° C. and mucobromic acid (6.82 g) in ethanol (10 mL) was added. After stirring at 50° C. for 1 h, a further portion of sodium ethoxide (10 mL of a 21% solution in ethanol) was added and the mixture was stirred at room temperature for 16 h. The mixture was then filtered and the filtrate reduced in vacuo. The residue was then treated with 2 M aqueous hydrochloric acid (30 mL) and stirred vigorously for 30 minutes. The resulting solid was filtered, washed with water and air dried to give 5-bromo-2-methyl-pyrimidine-4-carboxylic acid (1.46 g). This was then heated at 175° C. for 16 h. After cooling to room temperature the mixture was purified by Kugelrohr distillation to give 5-bromo-2-methyl-pyrimidine as a white solid (746 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383620B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-9cbfc31e361648e0a7a4ffb10d1c6fd4
출처 메모uspto-grants-2013_02