関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrothiopyran-4-one | HCID 66173 | — |
| 反応物 | 2-Amino-4-(trifluoromethyl)benzonitrile | HCID 13439028 | — |
| 触媒 | Zincchloride | HCID 3007855 | — |
| 溶媒 | Nitrobenzene | HCID 7416 | — |
| 生成物 | 10-amino-3,4-dihydro-7-trifluoromethyl-1H-thiopyrano[4,3-b]quinoline | HCID 14580248 | 54.7% |
反応手順
To a solution of 4-trifluoromethyl anthranilonitrile (12.2 g) in 50 ml of nitrobenzene was added freshly fused and pulverized zinc chloride (13.4 g). This was stirred at 50° C. for 1.5 hours after which was added tetrahydrothiopyran-4-one (9.9 g). The reaction mixture was stirred at 130° C. for 2 hours and allowed to cool, and the resulting complex was filtered and rinsed with ethyl ether. The solid was partitioned between 2-butanone (MEK) and NH4OH and the aqueous phase was extracted with MEK (2x). The organics were washed with water, dried (saturated NaCl, MgSO4) and concentrated to give 10.2 g of a yellow powder m.p. 253°-259° C.d. A 3.7 g portion was recrystallized from methanol/water to give 3.0 g of an off-white powder, m.p. 258°-262° C. d.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05112830 |
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| 出典データセット | uspto-grants-1992_05 |
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| ORD ID | ord-9d60d9b8daa6406d8165a3c64dbfa6df |
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| 出典メモ | uspto-grants-1992_05 |
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