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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 595080생성일: 2026년 10월 24일

Dimethylamine → 3-(5,5-Dimethyl-7-oxo-4,5,6,7-tetrahydro-benzothiazol-2-yl)-1,1-dimethyl-urea

https://huagongshe.com/ko/reaction/595080

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-oneHCID 587874—
용매AcetonitrileHCID 6342—
생성물3-(5,5-Dimethyl-7-oxo-4,5,6,7-tetrahydro-benzothiazol-2-yl)-1,1-dimethyl-ureaHCID 2050433082.3%

반응 조건

온도100 °C

반응 단계

To a solution of 2-amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one (151 g, 0.768 mol) in acetonitrile (5 L) are added CDI (249 g, 1.53 mol) and DBU (233 g, 1.53 mol). The reaction mixture is stirred overnight at 100° C. Dimethylamine (310 g, 3.83 mol) is added at RT and the stirring is continued overnight at 100° C. After cooling to RT, the reaction mixture is concentrated in vacuo and the residue is poured into ice water. The pH of the mixture is adjusted to pH 5 with HCl (6 M). The aqueous mixture is extracted with ethyl acetate (4×500 mL). The combined organic layers are washed with brine (500 mL) and dried over anhydrous Na2SO4. The solvent is evaporated in vacuo to give crude product. The crude product is washed with water to give 3-(5,5-dimethyl-7-oxo-4,5,6,7-tetrahydro-benzothiazol-2-yl)-1,1-dimethyl-urea (169 g, 82% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09243000B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-6999cae8d4f342d0ae16606ad2a34978
출처 메모uspto-grants-2016_01