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HRID 81986作成日:2026年10月24日

Triethylamine → 7-(3,5-Dimethylisoxazol-4-yl)-6-methoxy-N-(1-methoxypropan-2-yl)-3-nitroquinolin-4-amine

https://huagongshe.com/ja/reaction/81986

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物MethoxyisopropylamineHCID 123458—
反応物4-(4-Chloro-6-methoxy-3-nitroquinolin-7-yl)-3,5-dimethylisoxazoleHCID 57465580—
溶媒WaterHCID 962—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物7-(3,5-Dimethylisoxazol-4-yl)-6-methoxy-N-(1-methoxypropan-2-yl)-3-nitroquinolin-4-amineHCID 7098050493%

反応手順

1-(Methyloxy)-2-propanamine (0.35 g) and 4-chloro-7-(3,5-dimethyl-4-isoxazolyl)-6-(methyloxy)-3-nitroquinoline (for a preparation see Intermediate 8) (0.74 g, 2.217 mmol) were dissolved in a mixture of triethylamine (0.30 ml, 2.2 mmol) and NMP (3 ml) and the solution was allowed to stand for 30 min at room temperature, then diluted with water (20 ml) and the resulting suspension stirred for 20 min, then filtered and the resulting solid washed with water (10 ml) and dried in the vacuum oven at 50° C. to give the title compound as bright yellow solid. (0.80 g, 2.070 mmol, 93% yield). LCMS (formate) Rt 0.97 MH+ 387

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846709B2
出典データセットuspto-grants-2014_09
ORD IDord-f38cf3b8a8294bdb8d82abf63fdbd1ec
出典メモuspto-grants-2014_09