関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | N-(3-Chloropropyl)dibutylamine | HCID 96084 | — |
| 反応物 | 3-(4-Hydroxybenzoyl)-8-methylimidazo[1,2-a]pyridine | HCID 14201455 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(4-Dibutylaminopropoxybenzoyl)-8-methylimidazo[1,2-a]pyridine | HCID 10273738 | — |
反応手順
A mixture of 3-(4-hydroxybenzoyl)-8-methylimidazo[1,2-a]-pyridine (2.3 g, 9.6 mmol), dibutylaminopropyl chloride (6.8 g, 33 mmol) and potassium hydroxide (1.3 g, 23 mmol) in methanol (60 ml) was stirred at reflux for 96 hours. The mixture was concentrated and the resulting oil was flash chromatographed (silica gel, 2.5% methanol in diethyl ether) to give 1.3 g (31% yield) of the free base of the title compound. The HCl salt was prepared by dropwise addition of concentrated hydrochloric acid to a solution of the free base in methanol, concentrated and recrystallized from acetone-ether to give the HCl salt of the title compound as an off-white solid, mp 105° C. to 107° C. lR(KBr): 3440, 2640, 1645, 1605 cm-1. MS: 421 (M+). 1H NMR (CD3OD): δ9.66 (d, J=8 Hz, 1H), 8.74 (s, 1H), 8.00-7.61 (m, 4H), 7.20 (d, J=7.2 Hz, 2H), 4.29 (t, J=5 Hz, 2H), 3.41-3.15 (m, 6H), 2.75 (s, 3H), 2.31 (m, 2H), 1.80-1.42 (m, 8H), 1.02 (m, 6H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04727145 |
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| 出典データセット | uspto-grants-1988_02 |
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| ORD ID | ord-79b7e20c21f04bd287a87a9adaed0cfb |
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| 出典メモ | uspto-grants-1988_02 |
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