関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bis(2-bromoethyl) ether | HCID 21521 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | HCID 178516948 | HCID 178516948 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | HCID 178518177 | HCID 178518177 | — |
反応手順
To the mixture of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one (840 mg, 4.0 mmol) in THF (5.0 mL) was added LDA (2.0 M, 20 mL) at −78° C. The resulting mixture was stirred for 10 min at −78° C., and then 1-bromo-2-(2-bromoethoxy)ethane (3.71 g, 16 mmol) was added. The mixture was allowed to warm to room temperature and then stirred overnight. A sat'd solution of NaH2PO4 was added, and it was extracted with EtOAc. The organic layer was washed with sat'd NH4Cl, dried over MgSO4, filtered, and concentrated in vacuo. The crude residue was purified through flash chromatography (4:1:0.05; CH2Cl2/EtOAc/MeOH) to give the title compound as off-white solid. MS (ES+): 281 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08541592B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-d9390a08a4fb4fd890ff708357bfb600 |
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| 出典メモ | uspto-grants-2013_09 |
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