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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383874생성일: 2026년 10월 26일

Diisopropylethylamine → 3-Bromo-4-methyl-N-(4-(2-(pyrrolidin-1-yl)ethyl)phenyl)benzamide

https://huagongshe.com/reaction/383874

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3-Bromo-4-methylbenzoic acidHCID 82130—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물4-(2-(Pyrrolidin-1-yl)ethyl)anilineHCID 6487047—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-Bromo-4-methyl-N-(4-(2-(pyrrolidin-1-yl)ethyl)phenyl)benzamideHCID 68466263—

반응 단계

DIEA (473 μL, 2.72 mmol) was added into a solution of 3-bromo-4-methylbenzoic acid (189 mL, 0.881 mmol), 4-(2-(pyrrolidin-1-yl)ethyl)benzenamine (140 mg, 0.734 mmol), BOP (487 mg, 1.01 mmol) in DMF. The reaction mixture was stirred at rt under argon atmosphere overnight. The reaction mixture was diluted with AcOEt, and then washed with 1N NaOH aqueous solution three times. Organic phase was dried with anhydrous Na2SO4, and then evaporated to remove organic solvents. The obtained residue was further dried under high vacuum overnight to give crude product, which was used directly for the next step synthesis without further purification. MS (ESI+) m/z 387.0 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367686B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-94eccdfc318446c4999523b828f85fbe
출처 메모uspto-grants-2013_02