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HRID 2190394作成日:2026年10月25日

Bromine → N-{3-[(2-amino-1,3-benzothiazol-6-yl)oxy]phenyl}-3-(1-cyano-1-methylethyl)benzamide

https://huagongshe.com/reaction/2190394

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物Potassium thiocyanateHCID 516872—
反応物HCID 57386827HCID 57386827—
溶媒Acetic AcidHCID 176—
生成物N-{3-[(2-amino-1,3-benzothiazol-6-yl)oxy]phenyl}-3-(1-cyano-1-methylethyl)benzamideHCID 5738733187.2%

反応手順

To a solution of potassium thiocyanate (8.09 g, 83.2 mmol) in acetic acid (150 ml) was added a solution of N-[3-(4-aminophenoxy)phenyl]-3-(1-cyano-1-methylethyl)benzamide (7.34 g, 19.8 mmol) in acetic acid (150 ml), and the mixture was stirred at room temperature for 15 min. To the obtained solution was added dropwise a solution of bromine (4.0 g, 25.0 mmol) in acetic acid (100 mL) at room temperature over 30 min or longer and, after the completion of the dropwise addition, the mixture was stirred at room temperature for 4 hr. The resulting yellow solid was filtered off, and the filtrate was concentrated under reduced pressure. The residue was dissolved in tetrahydrofuran (100 mL) and ethyl acetate (200 mL), and basified with 2N aqueous sodium hydroxide solution. The aqueous layer was separated and the organic layer was washed with saturated aqueous ammonium chloride solution (200 mL), and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (7.4 g, 87%) as a yellow amorphous substance. The obtained compound was used in the next reaction without a further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08324395B2
出典データセットuspto-grants-2012_12
ORD IDord-99be044498ca4da29663578cbc6790ab
出典メモuspto-grants-2012_12