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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1811083생성일: 2026년 10월 26일

1,2-Dichloroethane → 4-bromo-7-(4-methylpiperazine-1-carbonyl)-9H-carbazole-1-carboxamide

https://huagongshe.com/reaction/1811083

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-MethylpiperazineHCID 53167—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물5-bromo-8-carbamoyl-9H-carbazole-2-carboxylic acidHCID 59375082—
용매dichloromethane tetrahydrofuran DMFHCID 86642945—
생성물4-bromo-7-(4-methylpiperazine-1-carbonyl)-9H-carbazole-1-carboxamideHCID 4683352276.1%

반응 단계

A suspension of 5-bromo-8-carbamoyl-9H-carbazole-2-carboxylic acid (Intermediate 49-1, 1.84 g, 4.97 mmol), EDC (1.334 g, 6.96 mmol), and HOBT (1.066 g, 6.96 mmol) in THF-DCM-DMF (4:1:1) (124 mL) was treated with 1-methylpiperazine (1.656 mL, 14.91 mmol) and the mixture was stirred at rt for 3 days. The mixture was concentrated and the residue was partitioned between DCM and NaHCO3 (aq). The organic phase was washed with brine, dried and concentrated to afford an oil. This was purified by column chromatography (DCM-2 M methanolic ammonia, 100:0 to 95:5 to 92.5:7.5). The resulting solid was suspended in EtOAc, collected by filtration and dried to provide 4-bromo-7-(4-methylpiperazine-1-carbonyl)-9H-carbazole-1-carboxamide (1.57 g, 76%). 1H NMR (400 MHz, DMSO-d6) δ 11.83 (s, 1H) 8.57 (d, J=8.13 Hz, 1H) 8.20 (br. s., 1H) 7.84 (d, J=8.35 Hz, 1H) 7.79 (s, 1H) 7.56 (br. s., 1H) 7.42 (d, J=8.13 Hz, 1H) 7.22 (d, J=8.13 Hz, 1H) 3.30-3.70 (m, 4H) 2.19-2.39 (m, 4H) 2.16 (s, 3H). Mass spectrum m/z 415, 417 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362065B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-691362b625a443439bceff99dec500ac
출처 메모uspto-grants-2013_01