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HRID 9117作成日:2026年10月26日

Trifluoromethanesulfonic anhydride → 1-(6-Bromo-7-trifluoromethylsulfonyl-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/reaction/9117

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物1-(6-Bromo-7-hydroxy-2-benzothiazolyl)-3-ethylureaHCID 21985595—
溶媒PyridineHCID 1049—
生成物1-(6-Bromo-7-trifluoromethylsulfonyl-2-benzothiazolyl)-3-ethylureaHCID 21985507—

反応条件

温度35 °C

反応手順

To a solution of 1-(6-bromo-7-hydroxy-2-benzothiazolyl)-3-ethyl-urea (50 mg, 0.158 mmol) in pyridine (1 mL) were added 3 portions of (CF3SO2)2O (29 μL, 0.174 mmol) about 45 minutes apart. The reaction mixture was stirred for about 3 hours at about 35° C. The solvent was then evaporated. The crude material was purified by LC/MS to give 23 mg (32%) pure 14. 1H NMR (DMSO) δ 1.09 (t, 3H, J=8 Hz CH3), 3.19 (m, 2H, CH2), 6.79 (br s, 1H, NH), 7.67 (d, 1H, J=12 Hz, ArH), 7.80 (d, 1H, J=8 Hz, ArH), 11.20 (br s, 1H, NH). HPLC retention time 3.58 minutes.

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-871ba8cd3b864435860dd69669537659
出典メモuspto-grants-2006_08