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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2056887생성일: 2026년 10월 25일

Phosgene → N-(3,4-dimethylbenzyl)-N'-(3-methyl-5-isoquinolinyl)urea

https://huagongshe.com/reaction/2056887

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물Benzenemethanamine, 3,4-dimethyl-HCID 66888—
반응물DiisopropylethylamineHCID 81531—
반응물3-Methylisoquinolin-5-amineHCID 12212055—
용매TolueneHCID 1140—
생성물N-(3,4-dimethylbenzyl)-N'-(3-methyl-5-isoquinolinyl)ureaHCID 9996072—

반응 단계

3,4-Dimethylbenzylamine (0.3 mL, 2.1 mmol) in toluene (11 mL) was added carefully to a 20% w/v solution of phosgene in toluene (4.5 mL). The mixture was refluxed overnight and was then concentrated in vacuo. The residue was then taken up in toluene (10 mL) and treated with DIEA (1.5 mL, 8.63 mmol) and 5-amino-3-methylisoquinoline (155 mg, 1.08 mmol). The reaction mixture was stirred at 80° for 2 h and was then cooled to room temperature. The precipitated solid was collected by filtration and was chromatographed on silica gel (97:3 CH2Cl2—CH3OH to 9:1 CH2Cl2—CH3OH, eluant gradient) to afford the desired product, A-473191. Treatment of this solid with methanolic HCl yielded the corresponding hydrochloride salt. 1H NMR (300 MHz, DMSO-d6) δ 9.16 (s, 1H), 8.59 (s, 1H), 8.24 (d, 1H, J=7.8 Hz), 7.74 (s, 1H), 7.68 (d, 1H, J=8.2 Hz), 7.50 (t, 1H, J=7.9 Hz), 7.08-7.12 (m, 3H), 6.95 (m, 1H), 4.28 (d, 2H, 5.8 Hz), 2.64 (s, 3H), 2.22 (s, 3H), 2.20 (s, 3H); MS (ESI30 ) m/z 320 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07335678B2
출처 데이터셋uspto-grants-2008_02
ORD IDord-460a3a5b640040d6907e5b3c246cb8ed
출처 메모uspto-grants-2008_02