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HRID 887268作成日:2026年10月27日

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

https://huagongshe.com/reaction/887268

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物Benzenemethanamine, 3,4-dimethyl-HCID 66888—
反応物DiisopropylethylamineHCID 81531—
反応物3-Methylisoquinolin-5-amineHCID 12212055—
溶媒TolueneHCID 1140—
生成物N-(3,4-dimethylbenzyl)-N'-(3-methyl-5-isoquinolinyl)ureaHCID 9996072—

反応手順

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 (ESI+) m/z 320 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08247413B2
出典データセットuspto-grants-2012_08
ORD IDord-f960ed20a3224f3ca796b588fe09ff0e
出典メモuspto-grants-2012_08