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HRID 9145作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Boric AcidHCID 7628—
反応物Sodium BicarbonateHCID 516892—
反応物3-Aminophenylboric acidHCID 21895836—
反応物1-(6-Bromo-2-benzothiazolyl)-3-ethylureaHCID 21985564—
触媒HCID 178418397HCID 178418397—
溶媒MethanolHCID 887—
溶媒N,N-Dimethylformamide--water (1/1)HCID 21962138—
生成物1-(6-(3-Aminophenyl)-2-benzothiazolyl)-3-ethylureaHCID 2198557523.4%

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091227B2
出典データセットuspto-grants-2006_08
ORD IDord-1d4c968dd1784c18a9903db176fc40d0
出典メモuspto-grants-2006_08