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HRID 524992作成日:2026年10月23日

Aniline → 3-Bromo-N-phenyl-1-(phenylsulfonyl)-1H-pyrrole-2-carboxamide

https://huagongshe.com/ja/reaction/524992

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物Sodium tartrate-2-hydrateHCID 517351—
反応物TrimethylaluminumHCID 16682925—
反応物Methyl 3-bromo-1-(phenylsulfonyl)-1H-pyrrole-2-carboxylateHCID 44518095—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物3-Bromo-N-phenyl-1-(phenylsulfonyl)-1H-pyrrole-2-carboxamideHCID 70978971114.7%

反応手順

In a three-necked round-bottom flask aniline (1.57 mL, 17.20 mmol) was dissolved in 80 mL of toluene under inert atmosphere. To this solution was added trimethy aluminium (7.82 mL, 15.64 mmol) and the mixture was stirred at room temperature during 10 minutes. Afterwards, a solution methyl 3-bromo-1-(phenylsulfonyl)-1H-pyrrole-2-carboxylate (2.0 g, 5.81 mmol) in 20 mL of toluene were added and the reaction mixtures was heated at 80° C. for 3 h. Next, the mixture was allowed to cool to room temperature and 20-30 mL of water was added to hydrolyze unreacted trimethyl aluminium and a 0,5M aqueous solution of disodium tartrate dihydrate was also added. After stirring for a while, the two layers were separated and the aqueous phase was extracted with ethyl acetate. The organic mixture was washed with the same 0,5M aqueous solution of disodium tartrate dehydrate (200 mL), water and brine, dried and concentrated in vacuum to afford 2.7 g of a residue that was used in the following step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340547B2
出典データセットuspto-grants-2016_05
ORD IDord-434824392d9f4be38e6a4fad389651c9
出典メモuspto-grants-2016_05