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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9145생성일: 2026년 10월 23일

Boric Acid → 1-(6-(3-Aminophenyl)-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/ko/reaction/9145

반응식

참여 물질

역할이름HCID투입량
반응물Boric AcidHCID 7628—
반응물Sodium BicarbonateHCID 516892—
반응물3-Aminophenylboric acidHCID 21895836—
반응물1-(6-Bromo-2-benzothiazolyl)-3-ethylureaHCID 21985564—
촉매HCID 178418397HCID 178418397—
용매MethanolHCID 887—
용매N,N-Dimethylformamide--water (1/1)HCID 21962138—
생성물1-(6-(3-Aminophenyl)-2-benzothiazolyl)-3-ethylureaHCID 2198557523.4%

반응 조건

온도100 °C

반응 단계

A suspension of 1-(6-bromo-2-benzothiazolyl)-3-ethylurea (0.300 g, 1.00 mmol), 3-aminophenyl boric acid (0.237 g, 1.50 mmol, 1.5 eq), and sodium bicarbonate (0.210 g, 2.50 mmol, 2.5 eq) in 8 mL of mixed solvent DMF/water (5/1) was purged with nitrogen gas. To the mixture, the catalyst Pd(PPh3)4 (0.058 g, 0.05 mmol, 0.05 eq) was added. It was purged with nitrogen gas again, and was heated at about 100° C. in a sealed tube for about 48 hours. More Pd(PPh3)4 (0.025 g, 0.02 mmol, 0.02 eq) and more boric acid (0.080 g, 0.50 mmol, 0.50 eq) were added after the first 24 hours. The mixture was taken up in MeOH, concentrated, dissolved in methylene chloride, washed with sodium bicarbonate solution, dried (MgSO4), evaporated, and purified by flash chromatography on SiO2 with MeOH and methylene chloride (1/50) to give the desired compound 0.073 g (23%). LC/MS 313.2 (M+1); LC retention time 2.11 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091227B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-1d4c968dd1784c18a9903db176fc40d0
출처 메모uspto-grants-2006_08