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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1876834생성일: 2026년 10월 27일

Dimethylcarbamoyl Chloride → 3-(1,7-Diphenyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-9-yl)-1,1-dimethylurea

https://huagongshe.com/reaction/1876834

반응식

참여 물질

역할이름HCID투입량
반응물Dimethylcarbamoyl ChlorideHCID 6598—
반응물TriethylamineHCID 8471—
반응물1,7-Diphenyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-9-amineHCID 2902530—
용매DichloromethaneHCID 6344—
생성물3-(1,7-Diphenyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-9-yl)-1,1-dimethylureaHCID 4448242449.4%

반응 단계

To a solution 1,7-diphenyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-9-amine (Intermediate 4), (106 mg, 0.31 mmol) in dichloromethane (10 mL) was added triethyl amine (0.130 mL, 0.933 mmol) followed by dimethylcarbamic chloride (0.043 mL, 0.46 mmol), under argon at 0° C. The reaction mixture was then stirred at room temperature for overnight. The mixture was quenched with water (30 mL). The residue was isolated in a typical aqueous workup and purified by MPLC (medium pressure liquid chromatography) using silica gel column with 10 to 15% EtOAc:Hexane to give 3-(1,7-diphenyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-9-yl)-1,1-dimethylurea, (405), (63 mg 49%). 1H NMR (300 MHz, CDCl3) ppm 2.01-2.16 (m, 2H) 2.20-2.37 (m, 2H) 2.85 (s, 6H) 3.00-3.15 (m, 4H) 4.12-4.25 (m, 2H) 5.78 (s, 1H) 6.62 (s, 2H) 7.10-7.22 (m, 5H) 7.23-7.34 (m, 5H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309729B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-4400d0dd4a0943df9614fc814aa51774
출처 메모uspto-grants-2012_11