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HRID 989340作成日:2026年10月26日

Acetic Acid → 7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile

https://huagongshe.com/reaction/989340

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物AcetonitrileHCID 6342—
反応物ButyllithiumHCID 178418339—
反応物HCID 178496951HCID 178496951—
溶媒TetrahydrofuranHCID 8028—
生成物7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrileHCID 9813663—

反応条件

温度-78 °C

反応手順

To a solution of 4.75 mL (11.88 mmol) of n-butyllithium (2.5M in hexane) in 4.0 mL of tetrahydrofuran at −78° C. is added dropwise a solution of 0.68 mL (13.1 mmol) of acetonitrile in 6.8 mL of tetrahydrofuran. After completion of addition, the suspension is stirred for 10 minutes. To this is added 1.36 g (4.75 mmol) of methyl 3-{[(E)-(dimethylamino)methylidene]amino}-7-methoxy-2-naphthoate in 32 mL of tetrahydrofuran dropwise. The resulting reaction mixture is stirred at −78° C. for 1 hour, at −5° C. for 1 hour and at room temperature for 15 minutes. The reaction mixture is again cooled to −78° C. and 1.72 g (28.6 mmol) of acetic acid is added dropwise. After addition of the acetic acid, the reaction mixture is allowed to warm to room temperature. The precipitate is collected by filtration and washed sequentially with water, acetonitrile and methanol. After drying in vacuo, this yields 796.9 mg (67%) of 7-methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile as a deep yellow solid, mp>260° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06638929B2
出典データセットuspto-grants-2003_10
ORD IDord-e64447100648458bb0aacd9594b0b3c2
出典メモuspto-grants-2003_10