関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 3-Bromoazocan-2-one | HCID 567205 | — |
| 反応物 | Tert-butyl 2-iodoacetate | HCID 11021060 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-t-Butoxycarbonylmethyl-3-bromoperhydroazocin-2-one | HCID 13188852 | — |
反応手順
To a vigorously stirred suspension of 0.55 g sodium hydride in 30 ml tetrahydrofuran add over 20 min. a solution of 5.0 g t-butyl iodoacetate and 4.12 g 3-bromoperhydroazocin-2-one [Nagasawa et al., J. Med. Chem., 14 501 (1971)] dissolved in 35 ml tetrahydrofuran. After the addition is completed stir the reaction at room temperature for 1.5 hours then quench by the addition of 5-6 ml of saturated NH4Cl solution. Filter the reaction and concentrate the filtrate. Add ether to the residue, filter and wash the filtrate with H2O and brine. Dry the ether solution and concentrate to obtain 1-t-butoxycarbonylmethyl-3-bromoperhydroazocin-2-one. Prepare an analytical sample by silica gel chromatography. M.p. 107.5-109. Anal. (C13H22BrNO3). Calc: C, 48.75; H, 6.93; N, 4.37. Found: C, 48.78; H, 7.12; N, 4.26.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04396616 |
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| 出典データセット | uspto-grants-1983_08 |
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| ORD ID | ord-df64c936db6c430aa36a96caf445b484 |
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| 出典メモ | uspto-grants-1983_08 |
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