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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36388생성일: 2026년 10월 23일

2-Amino-4,6-dimethoxypyrimidine → Amidosulfuron

https://huagongshe.com/ko/reaction/36388

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4,6-dimethoxypyrimidineHCID 118946—
반응물1-[(N-methylsulfonyl-N-methylamino)-sulfonyl]-3-(N-methylsulfonyl-N-methylamino)ureaHCID 23373886—
용매ChlorobenzeneHCID 7964—
생성물AmidosulfuronHCID 91777103.2%

반응 조건

온도80 °C

반응 단계

32.3 g of 1-[(N-methylsulfonyl-N-methylamino)-sulfonyl]-3-(N-methylsulfonyl-N-methylamino)urea are slurried in 500 ml of chlorobenzene, 15.5 g of 2-amino-4,6-di-methoxypyrimidine are added at 80° C. with stirring, and the mixture is heated for 3 hours at 80° C. After cooling to 20° C., the precipitate is filtered off and washed with 100 ml of chlorobenzene. 36.4 g of the desired product are obtained with a purity of 98.1%, corresponding to a yield of 96.8% of theory. The melting point for the product is 183°-185° C. 5.1 g of N-methylmethanesulfonamide are recovered from the filtrate by distillation, corresponding to a yield of 92.7% of theory.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05414084
출처 데이터셋uspto-grants-1995_05
ORD IDord-06b25bb0346b4fd7a734e7384a16ca50
출처 메모uspto-grants-1995_05