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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1419736생성일: 2026년 10월 26일

N,N-Dimethylcyclohexylamine → 6-chloro-N-(3-methylbutan-2-yl)-1,1-dioxo-4H-thieno[3,2-e][1,2,4]thiadiazin-3-amine

https://huagongshe.com/reaction/1419736

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylcyclohexylamineHCID 7415—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물3-Methylbutan-2-amine--hydrogen chloride (1/1)HCID 120793—
반응물6-chloro-2,3-dihydro-3-oxo-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-dioxideHCID 11096689—
용매WaterHCID 962—
생성물6-chloro-N-(3-methylbutan-2-yl)-1,1-dioxo-4H-thieno[3,2-e][1,2,4]thiadiazin-3-amineHCID 1784462967%

반응 조건

온도200 °C

반응 단계

Phosphorus pentoxide (2.84 g; 20 mmol), N,N-dimethylcyclohexylamine (5 ml, 33 mmol) and 1,2-dimethylpropylamine hydrochloride (2.47 g; 20 mmol) were carefully mixed in a three necked flask equipped with mechanical stirring and condenser with drying tube. The mixture was heated on an oil bath at 200° C. until a homogeneous mass was obtained. Then 6-chloro-2,3-dihydro-3-oxo-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-dioxide (1.2 g; 5 mmol) was added and the mixture was stirred at 240° C. for 45 min. The mixture was allowed to cool to about 100° C., 150 ml of water was added and stirring was continued at ambient temperature for approximately 1 h. The hydrolysed mixture was filtered and the dark precipitate was washed with water and dissolved in boiling ethanol, treated with charcoal, filtered and finally evaporated to dryness. Flash chromatography (ethyl acetate/silica gel) afforded 105 mg (7%) of the pure title compound; m.p. 216°-218° C.; 1H-NMR (DMSO-d6): δ 0.90 (d, 6H, CH(CH3)2), 1.08 (d, 3H, NCHCH3), 1.75 (m, 1H, CH(CH3)2), 3.65 (m, 1H, NHCH), 7.11 (br. s, 2H, 5-H+NH), 10.68 (s, 1H, NH); MS m/e: 307/309 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05889002
출처 데이터셋uspto-grants-1999_03
ORD IDord-7a6d6969eb934f178aac4cdfdb5bad94
출처 메모uspto-grants-1999_03