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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9104생성일: 2026년 10월 24일

Formaldehyde → N-(6-Cyano-1,3-benzothiazol-2-yl)-N'-(3-pyridylmethyl)urea

https://huagongshe.com/ko/reaction/9104

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물MethylamineHCID 6329—
반응물4-MethylmorpholineHCID 7972—
반응물N-Ethyl-N'-(6-nitro-1,3-benzothiazol-2-yl)ureaHCID 9813955—
반응물1-Ethyl-5-methyl-3-(6-nitro-1,3-benzothiazol-2-yl)-1,3,5-triazinan-2-oneHCID 21985532—
용매MethanolHCID 887—
용매Water ethanolHCID 19096565—
생성물N-(6-Cyano-1,3-benzothiazol-2-yl)-N'-(3-pyridylmethyl)ureaHCID 21985518—

반응 조건

온도80 °C

반응 단계

General procedure for synthesizing 1-ethyl-5-methyl-3-(6-nitro-1,3-benzothiazol-2-yl)-1,3,5-triazinan-2-one: N-Ethyl-N′-(6-nitro-1,3-benzothiazol-2-yl)urea is suspended in an alkanol/water mixture, preferably 1:1 EtOH/H2O at room temperature. A 37% aqueous solution of formaldehyde is added followed by addition of a 2M solution of MeNH2 in MeOH, then about 2 mole equivalents of N-methylmorpholine. The solution is warmed to about 70–85° C., preferably 80° C., then allowed to stir for about 4–24 hours, preferably 4 hours. The slurry is then cooled to room temperature, filtered and washed well with water, dried and the title product is isolated. General Procedure for Grignard Addition:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091227B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-e8b7ee04ec75448d86e69b5a0568d5fc
출처 메모uspto-grants-2006_08