関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Glycol monoethyl ether | HCID 8076 | — |
| 反応物 | (3-Amino-2-methylphenyl)methanol | HCID 577175 | — |
| 反応物 | Pyridinium chloride | HCID 10176127 | — |
| 反応物 | 4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrile | HCID 10586676 | — |
| 生成物 | 4-(3-Hydroxymethyl-2-methylphenylamino)-6,7-dimethoxyquinoline-3-carbonitrile | HCID 22466580 | 91.6% |
反応手順
A mixture of 0.248 g (1 mmol)of 4-chloro-6,7-dimethoxy-quinoline-3-carbonitrile, 0.151 g (1.1 mmol) of 3-amino-2-methylbenzyl alcohol, 0.116 g (1 mmol) pyridine hydrochloride and 12 ml of 2-ethoxyethanol was heated in a 138-140° C. oil bath for 6 hours; progress of the reaction was monitored by TLC. When TLC indicated the disappearance of starting material, the reaction was cooled and concentrated in vacuo to a thick oil. To this oil was added 50 ml of water followed by 5 ml of 1M NaHCO3, approximately pH 8. The resulting precipitate was collected, washed with water and diethyl ether, and dried in vacuo at 65° C. to give 0.32 g (91.5%) of the desired product as light tan crystals. MP 123-125° C.;: mass spectrum (electrospray, m/e,): 349.9(M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06384051B1 |
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| 出典データセット | uspto-grants-2002_05 |
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| ORD ID | ord-6ee170aa84154a799f6dcb9bd5c81ca3 |
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| 出典メモ | uspto-grants-2002_05 |
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