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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10799생성일: 2026년 10월 25일

Cyanamide → [4-Amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl](2,3-dihydro-1,4-benzodioxin-6-yl)methanone

https://huagongshe.com/reaction/10799

반응식

참여 물질

역할이름HCID투입량
반응물CyanamideHCID 9864—
반응물2-Bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethan-1-oneHCID 2776171—
반응물1-(4-Isothiocyanatophenyl)-4-methylpiperazineHCID 13718397—
반응물Potassium tert-butoxideHCID 23665647—
용매AcetonitrileHCID 6342—
용매tert-ButanolHCID 6386—
생성물[4-Amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl](2,3-dihydro-1,4-benzodioxin-6-yl)methanoneHCID 991165266%

반응 단계

tert-Butanol (4 mL) and then 1-(4-isothiocyanatophenyl)-4-methyl piperazine (of Example 1; 219 mg, 1 mmol) were added to a solution of cyanamide (44 mg, 1.05 mmol) (Aldrich) in acetonitrile (5 mL). Potassium t-butoxide (1 M in tert-butanol; 1 mL, 1 mmol) was added and the solution was stirred for 30 min. 2-Bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethanone (257 mg, 1 mmol) (Maybridge Chemical Company Ltd.) was added, and the solution was stirred at room temperature for 3 days. The yellow solid was filtered off and washed with cold acetonitrile and then ether to give [4-amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl](2,3-dihydro-1,4-benzodioxin-6-yl)methanone (280 mg, 66%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094896B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4444a9b30ad444b689cb68b79a2ae3f2
출처 메모uspto-grants-2006_08