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7-Chloro-2-(chloromethyl)quinoline → 7-Chloro-2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline hydrogen chloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 7-Chloro-2-(chloromethyl)quinoline | HCID 10954844 | — |
| 反応物 | Methyl 4-(2-quinolinylmethoxy)benzoate | HCID 19934817 | — |
| 反応物 | 4-[1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl]Phenol | HCID 135915213 | — |
| 生成物 | 7-Chloro-2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline hydrogen chloride | HCID 11561731 | — |
反応手順
Following the procedure for the preparation of 4-(Quinolin-2-ylmethoxy)-benzoic acid methyl ester but substituting 4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenol and 7-chloro-2-chloromethyl-quinoline provided the title compound. 1H NMR (400 MHz, DMSO) δ 8.66 (d, J=6.6 Hz, 2H), 8.54 (s, 1 H), 8.47 (d, J=8.3, 2H), 8.04 (m, 2H), 7.70 (m, 2H), 7.65 (m, 1H), 7.36 (d, J=8.7 Hz, 2H), 7.12 (d, J=8.7, 2H), 5.38 (s, 2H), 3.90 (s, 3 H); MS: (M+H m/z=427.1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07429665B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-691d24d58cb347c197930b510ed1a33c |
| 出典メモ | uspto-grants-2008_09 |