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HRID 2089545作成日:2026年10月27日

Phosgene → 1-Cyclopropyl-3-[3-(1,2,3,4-tetrahydro-naphthalen-1-yl)-3h-imidazol-4-yl]-urea

https://huagongshe.com/reaction/2089545

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物4-NitroimidazoleHCID 18208—
反応物CyclopropylamineHCID 69828—
反応物5-Nitro-1(1,2,3,4-tetrahydro-naphthalen-1-yl)-1h-imidazoleHCID 59199381—
触媒PalladiumHCID 23938—
生成物1-Cyclopropyl-3-[3-(1,2,3,4-tetrahydro-naphthalen-1-yl)-3h-imidazol-4-yl]-ureaHCID 59199336—

反応手順

In the first step a modified Mitsunobu reaction employing 5-nitro-1H-imidazole (CAS #3034-38-6) can be preformed as described in Example 1. The resulting 5-nitro-1(1,2,3,4-tetrahydro-naphthalen-1-yl)-1H-imidazole, can then be reduced via the employment of palladium on carbon under a hydrogen atmosphere. The resulting amine can undergo treatment with phosgene followed by the addition of cyclopropylamine to afford 1-cyclopropyl-3-[3-(1,2,3,4-tetrahydro-naphthalen-1-yl)-3H-imidazol-4-yl]-urea; MS: (ESI) m/z 297.1 (M+H)+; 1H NMR (400 MHz, CDCl3) δ ppm 0.46-0.57 (m, 2 H), 0.68-0.77 (m, 2 H), 1.78-2.29 (m, 4 H), 2.49-2.60 (m, 1 H), 2.79-3.01 (m, 2 H), 5.17-5.31 (m, 1 H), 5.34-5.43 (m, 1 H), 6.33-6.43 (m, 1 H), 6.85 (d, J=7.6 Hz, 1 H), 7.01 (s, 1 H), 7.13 (t, J=7.5 Hz, 1 H), 7.17-7.26 (m, 3 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08436035B2
出典データセットuspto-grants-2013_05
ORD IDord-2ee919f6629f41c885d0e1a98e54f52e
出典メモuspto-grants-2013_05