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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397415생성일: 2026년 10월 24일

1,2-Dichloroethane → 4-methyl-5-(4-methyl-piperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde

https://huagongshe.com/ko/reaction/397415

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-MethylpiperazineHCID 53167—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물5-Formyl-3-methyl-1H-pyrrole-2-carboxylic acidHCID 15694078—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-methyl-5-(4-methyl-piperazine-1-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 2239097666%

반응 단계

To a solution of 5-formyl-3-methyl-1H-pyrrole-2-carboxylic acid (306.3 mg, 2 mmol) in DMF 5 mL was added HOBt (324.3 mg, 2.4 mmol), EDC (460.1 mg, 2.4 mmol) and then 1-methylpiperazine (0.27 mL, 2.4 mmol). The mixture was stirred at room temperature under nitrogen for overnight. The reaction was diluted with ethyl acetate and washed with sodium bicarbonate. The aqueous layer was extracted several times with ethyl acetate. The combined organic layer was washed with brine, dried, concentrated and column chromatographed (MeOH/DCM) to give 310 mg (66%) of 4-methyl-5-(4-methyl-piperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde as a light yellow foam solid. 1H NMR (360 MHz, DMSO-d6) δ 12.20 (br s, 1H, NH), 9.47 (s, 1H, CHO), 6.80 (s, 1H), 3.58 (m, 4H, 2×CH2), 3.44 (m, 4H, 2×CHO, 2.03 (s, 3H, CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610688B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-78ac8d8d2b1b43829a1c4e5f0d7eb89b
출처 메모uspto-grants-2003_08