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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379563생성일: 2026년 10월 25일

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → 1-(6-Bromonaphth-2-ylsulphonyl)-4-[4-(2-methyl-4-pyridyl)benzoyl]piperazine

https://huagongshe.com/reaction/379563

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-(2-Methylpyridin-4-yl)benzoic acidHCID 18617748—
반응물1-(6-Bromonaphthalene-2-sulfonyl)piperazineHCID 22329709—
용매DimethylformamideHCID 6228—
생성물1-(6-Bromonaphth-2-ylsulphonyl)-4-[4-(2-methyl-4-pyridyl)benzoyl]piperazineHCID 2232973468%

반응 단계

4-(2-Methyl-4-pyridyl)benzoic acid (62 mg), 1-(6-bromonaphth-2-ylsulphonyl) piperazine (94 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (61 mg) were dissolved in DMF (2.5 ml) and the resultant solution stirred at ambient temperature for 16 hours. Excess DMF was removed in vacuo, water (10 ml) was added and the precipitate that formed was filtered, washed thoroughly with cold water and dried over P2O5. The solid thus obtained was purified by flash chromatography at 3 psi on silica (Merck ART 9385) eluting with 2.5% v/v methanol in dichloromethane. There was thus obtained the 1-(6-bromonaphth-2-ylsulphonyl)-4-[4-(2-methyl-4-pyridyl)benzoyl]piperazine (99 mg); mp 204-205° C.; 1H NMR (300 MHz, DMSO-d6) δ=2.48 (s,3H), 3.03 (s,4H), 3.57 (broad s, 4H), 7.46 (t,3H), 7.56 (s,1H), 7.77(d,2H), 7.83(d,2H), 8.17(q,2H), 8.42 (s,1H), 8.48 (d,2H), ppm; MS: m/z 550/552 (M+H)+ (1 Br pattern).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300330B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-b306ff9290864ff18c29d9944b253ab1
출처 메모uspto-grants-2001_10