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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247469생성일: 2026년 10월 26일

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-(3-Chloropyridazine-6-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea

https://huagongshe.com/reaction/247469

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
반응물N-(3-chloropyridazine-6-sulfonyl)phenylcarbamateHCID 86741701—
용매1,4-DioxaneHCID 31275—
생성물N-(3-Chloropyridazine-6-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)ureaHCID 2127574343.3%

반응 단계

A mixture of 14.2 g of N-(3-chloropyridazine-6-sulfonyl)phenylcarbamate and 6.3 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine are refluxed for 1 hour in 120 ml of absolute dioxan. When the reaction is complete, the mixture is concentrated in vacuo and the residue is taken up in a saturated aqueous solution of sodium bicarbonate and the insoluble constituents are extracted with methylene chloride. The aqueous phase is acidified with dilute hydrochloric acid and extracted with methylene chloride. The methylene chloride solution is dried over sodium sulfate and concentrated, affording 7 g of the compound of the above formula with a melting point of 135° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04707551
출처 데이터셋uspto-grants-1987_11
ORD IDord-cc3cf87295054356b17909d3b9a248d0
출처 메모uspto-grants-1987_11