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HRID 418990作成日:2026年10月27日

3-Amino-2-bromo-5-chloropyridine → N-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-3-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/reaction/418990

反応式

関与物質

役割名称HCID仕込み量
反応物3-Amino-2-bromo-5-chloropyridineHCID 2769640—
反応物4-Chloro-3-(trifluoromethyl)benzenesulfonyl ChlorideHCID 2780719—
溶媒PyridineHCID 1049—
生成物N-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-3-trifluoromethyl-benzenesulfonamideHCID 57942594—

反応条件

温度60 °C

反応手順

A mixture of 4-chloro-3-trifluoromethyl-benzenesulfonyl chloride (1.5 g, 5.3 mmol) and 2-bromo-5-chloro-pyridin-3-ylamine (500 mg, 2.4 mmol) dissolved in pyridine (20 mL) was heated at 60° C. for 16 h. The solvent was evaporated and the residue suspended in a 1:1 mixture of 2 M NaOH and methanol (20 mL) and heated at 70° C. for 30 min. The methanol was evaporated under reduced pressure and the residue diluted with 15 mL water. The solution was cooled on ice bath and the pH was adjusted to 3 by drop wise addition of concentrated HCl. The solid formed was collected by filtration and the product was purified by flash chromatography on silica gel column to afford the desired product. MS m/z: 450.8 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093247B2
出典データセットuspto-grants-2012_01
ORD IDord-bdf7097ebde54bb28fa3f5be240f6d06
出典メモuspto-grants-2012_01