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HRID 6430作成日:2026年10月23日

Boric Acid → 2-(1H-Pyrrol-2-yl)benzo[d]thiazole

https://huagongshe.com/ja/reaction/6430

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2-AminothiophenolHCID 8713—
反応物Pyrrole-2-Carboxylic AcidHCID 12473—
溶媒O-XyleneHCID 7237—
溶媒Ethyl AcetateHCID 8857—
生成物2-(1H-Pyrrol-2-yl)benzo[d]thiazoleHCID 13562548314%

反応手順

A mixture of 5.55 g (50 mmol) of pyrrole-2-carboxylic acid, 6.26 g (50 mmol) of 2-aminothiophenol and 3.09 g (50 mmol) of boric acid in 250 mL of xylene was heated under reflux for 3 days while removing water which was generated from reaction using a Dean-Stark trap. the cooled reaction mixture was diluted with 200 mL of ethyl acetate, washed with 200 mL of 5% sodium hydroxide solution and then with 200 mL of water. The separated organic layer was dried over anhydrous sodium sulfate. The resulting crude product was purified by column chromatography on silica gel with 10% ethyl acetate in hexane as eluant. The desired product, 2-(pyrrol-2-yl)benzothiazole (1.40 g, 14%) was obtained as a pale yellow solid. m.p. 150°-151° C.; 1H-NMR (CDCl3) 6.32-6.35 (m, 1H, ArH), 6.87-6.89 (m, 1H, ArH), 6.94-6.96 (m, 1H, ArH), 6.33 (t, 1H, ArH), 6.43 (t, 1H, ArH), 7.84 (d, 1H, ArH), 7.90 (d, 1H, ArH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248782
出典データセットuspto-grants-1993_09
ORD IDord-514be903fc7a4ed1b961eb5abfbc5505
出典メモuspto-grants-1993_09