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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1992739생성일: 2026년 10월 24일

Trifluoroacetic acid → 3,5-Dibromo-N-(2-methyl-3-phenyl-allyl)-N-[2-(1-methyl-pyrrolidin-2-yl)-ethyl]-benzamide

https://huagongshe.com/ko/reaction/1992739

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Benzoic acid, 3,5-dibromo-HCID 12063—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물(2-Methyl-3-phenyl-allyl)-[2-(1-methyl-pyrrolidin-2-yl)-ethyl]-amineHCID 68680591—
용매AcetonitrileHCID 6342—
용매TriethylamineHCID 8471—
생성물3,5-Dibromo-N-(2-methyl-3-phenyl-allyl)-N-[2-(1-methyl-pyrrolidin-2-yl)-ethyl]-benzamideHCID 6868272363%

반응 단계

An analogous procedure to Example 2 was used with 3,5-dibromo-benzoic acid 0.16 g (0.38 mmol) and (2-methyl-3-phenyl-allyl)-[2-(1-methyl-pyrrolidine-2-yl)-ethyl]-amine 0.1 g (0.38 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride 0.11 g (0.57 mmol), 1-hydroxybenzotriazole 0.05 g (0.41 mmol) and triethylamine 0.08 ml. Reverse phase prep HPLC with a gradient 20-80% for the acetonitrile phase gavel 53 mg as a TFA salt. Yield: 63%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07649011B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-35fdc6c84df143be8e1de87b274c755c
출처 메모uspto-grants-2010_01