関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | Benzenesulfonic Acid | HCID 7371 | — |
| 反応物 | 2,2-Difluoro-2-pyridin-2-ylethyl 4-methylbenzenesulfonate | HCID 58249642 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 溶媒 | Isopropyl Acetate | HCID 7915 | — |
| 生成物 | 2,2-difluoro-2-pyridin-2-yl-ethylamine benzenesulphonate, (1:1 salt) | HCID 78357863 | 49.5% |
反応手順
10 g of 2,2-Difluoro-2-pyridin-2-ylethyl 4-methylbenzenesulfonate (J) obtained in step 3, 5 g of NaI, 20 mL of DMSO and 90 mL of aqueous ammonia were taken in a 500 mL autoclave vessel. The reaction mixture was heated to 80° C. and a pressure of 15 to 17 kg of ammonia maintained for 30-40 hours. The volume of the reaction mass was reduced by vacuum distillation. The RM was washed with 60 mL of IPE. The pH of the RM was adjusted to 10-14 by adding a 50% NaOH solution and extracted three times with 60 mL of MDC. The combined MDC layers were washed with brine, dried over sodium sulphate and distilled under vacuum (crude weight=8 g). The crude mass obtained was dissolved with 10 mL of MDC, and to this 4.5 g benzene sulphonic acid (BSA) dissolved in 30 mL isopropyl acetate (IPAc) was added dropwise over a period of 30 minutes with stirring at RT. The RM was stirred for 30 minutes at RT. The solid obtained was filtered and washed with IPAc and dried under vacuum, resulting in 5 g of the titled compound (Yield=49.5%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08541580B2 |
|---|
| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-ac1aafe395f44b6fa336ed0ef1904144 |
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| 出典メモ | uspto-grants-2013_09 |
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