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HRID 1170346作成日:2026年10月26日

2-{4-[4-Pyridin-4-yl-1-(2,2,2-trifluoro-ethyl)-1H-pyrazol-3-yl]-phenoxymethyl}-quinoxaline → 4-Chloro-2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline

https://huagongshe.com/reaction/1170346

反応式

関与物質

役割名称HCID仕込み量
反応物2-{4-[4-Pyridin-4-yl-1-(2,2,2-trifluoro-ethyl)-1H-pyrazol-3-yl]-phenoxymethyl}-quinoxalineHCID 11554407—
反応物(4-Chloroquinolin-2-yl)methanolHCID 53800151—
反応物4-[1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl]PhenolHCID 135915213—
生成物4-Chloro-2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinolineHCID 11597089—

反応手順

Following the procedure for the preparation of 2-{4-[4-Pyridin-4-yl-1-(2,2,2-trifluoro-ethyl)-1H-pyrazol-3-yl]-phenoxymethyl}-quinoxaline but substituting 4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenol and (4-Chloro-quinolin-2-yl)-methanol provided the title compound. 1H NMR (400 MHz, CDCl3) δ 8.43 (d, J=4.6 Hz, 2H), 8.18 (d, J=8.7 Hz, 1H), 8.04 (d, J=7.9 Hz, 1H), 7.73 (m, 2H), 7.60 (t, J=7.1 Hz, 1H), 7.52 (s, 1H), 7.37 (d, J=9.1, Hz, 2H), 7.12 (d, J=6.2 Hz, 2H), 6.98 (d, J=8.7 Hz, 2H), 5.30 (s, 2H), 3.90 (s, 3H); MS: (M+H m/z=427.1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07825254B2
出典データセットuspto-grants-2010_11
ORD IDord-6eac6de15f174b40ac2fc649562d60e1
出典メモuspto-grants-2010_11