関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,2-Dichloro-1,1-difluoroethane | HCID 15442 | — |
| 反応物 | (tert-Butoxycarbonyl)homocysteine | HCID 18322443 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Sodium Hydroxide | HCID 14798 | — |
| 生成物 | N-Boc-S-(2-chloro-1,1-difluoroethyl)-D,L-homocysteine | HCID 18322437 | — |
反応手順
Ex-18a) A solution of N-Boc-D,L-homocysteine (5 mmol) in NaOH (5 mL, 2N) was slowly added to a stirred solution of 1,2-dichloro-1,1-difluoroethane (5 mmol) in DMF. The resulting solution was then warmed to 50° C. for 16 hours. The reaction solution was then poured onto EtOAc and extracted with citric acid (5%) and brine, dried (Na2SO4) and concentrated in vacuo. The material was purified by flash column chromatography to yield N-Boc-S-(2-chloro-1,1-difluoroethyl)-D,L-homocysteine. Example 18 is prepared in the same manner as described for Example 17 starting with N-Boc-S-(2-chloro-1,1-difluoroethyl)-D,L-homocysteine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06344483B1 |
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| 出典データセット | uspto-grants-2002_02 |
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| ORD ID | ord-150efa6fd236480789542d590f9ef718 |
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| 出典メモ | uspto-grants-2002_02 |
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