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HRID 524992생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물Sodium tartrate-2-hydrateHCID 517351—
반응물TrimethylaluminumHCID 16682925—
반응물Methyl 3-bromo-1-(phenylsulfonyl)-1H-pyrrole-2-carboxylateHCID 44518095—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3-Bromo-N-phenyl-1-(phenylsulfonyl)-1H-pyrrole-2-carboxamideHCID 70978971114.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340547B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-434824392d9f4be38e6a4fad389651c9
출처 메모uspto-grants-2016_05