戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 64332作成日:2026年10月24日

Phosphorous acid → 5-Amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

https://huagongshe.com/ja/reaction/64332

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorous acidHCID 107909—
反応物5-amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carbonitrileHCID 117668213—
生成物5-Amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamideHCID 117668233—

反応条件

温度100 °C

反応手順

A mixture of 5-amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carbonitrile (137 mg, 0.287 mmol) in phosphorous acid (85 wt. % in H2O, 10 mL) was stirred at 100° C. for 1 hr, until TLC and LCMS analysis showed that most of starting material was consumed. The reaction was cooled to room temperature and partitioned between water (40 mL) and EA (40 mL). Organic layer was separated from aqueous layer. The aqueous phase was then extracted with EA (20 mL). The combined organic layers were washed with brine (50 mL), dried over Na2SO4 and concentrated to get the crude product (149 mg) which was used in next step without further purification. MS (ESI) m/e [M+1]+494, 496.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447106B2
出典データセットuspto-grants-2016_09
ORD IDord-c4bb597513e8498b81f19dd0b55f5f5b
出典メモuspto-grants-2016_09