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Ammonium Chloride → (+)-N,N-diethyl-4-[{[(S)-(4-methylphenyl)sulfinyl]amino}(8-quinolinyl)methyl]-benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | N,N-diethyl-4-iodobenzamide | HCID 875218 | — |
| 反応物 | (NE,S)-4-methyl-N-(quinolin-8-ylmethylidene)benzenesulfinamide | HCID 87713000 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Tetrahydrofuran toluene | HCID 22635083 | — |
| 生成物 | (+)-N,N-diethyl-4-[{[(S)-(4-methylphenyl)sulfinyl]amino}(8-quinolinyl)methyl]-benzamide | HCID 69143830 | 23.1% |
反応条件
| 温度 | -78 °C |
|---|
反応手順
N,N-diethyl 4-iodo-benzamide (3.1 g, 10 mmol) was dissolved in dry toluene/THF (9:1, 200 mL) and cooled to −78° C. under nitrogen. n-BuLi (7.8 mL, 1.3 M in hexane, 10 mmol) was added dropwise during 5 to 10 min. After further 5 min, 3 (1.0 g, 3.4 mmol) was added dissolved in toluene (1 mL). The solution was stirred 10 min, then NH4Cl (aq.) was added. Concentration, aqueous workup and chromatography on silica gave a total of 0.70 g (44%) of a 70:30 mixture of diastereomers. The pure major isomer 5 (0.37 g) was obtained by one more chromatography. 1H NMR (CDCl3): δ1.2 (m, 6H), 2.4 (s, 3H), 3.4 (m, 4H), 6.35 (d, J=7.5 Hz, 1 H), 6.61 (d, J=7.5 Hz,1 H), 7.15-7.55 (m, 11H), 7.75 (m, 1H), 8.12 (m, 1H), 8.75 (m, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07423154B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-6e3ffd5e9a7547cc853c664e0f6bfd9f |
| 出典メモ | uspto-grants-2008_09 |