참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 반응물 | HCID 178496951 | HCID 178496951 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile | HCID 9813663 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06638929B2 |
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| 출처 데이터셋 | uspto-grants-2003_10 |
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| ORD ID | ord-e64447100648458bb0aacd9594b0b3c2 |
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| 출처 메모 | uspto-grants-2003_10 |
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