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Sodium Ascorbate → 4-[4-(4-Methanesulfonyl-phenoxymethyl)-[1,2,3]triazol-1-yl]-piperidine-1-carboxylic acid tert-butyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Ascorbate | HCID 23667548 | — |
| 反応物 | 1-(Methylsulfonyl)-4-(prop-2-ynyloxy)benzene | HCID 57708390 | — |
| 反応物 | 2-Methylpropan-2-ol--water (1/1) | HCID 71401949 | — |
| 反応物 | 4-Azido-piperidine-1-carboxylic acid | HCID 86674911 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-[4-(4-Methanesulfonyl-phenoxymethyl)-[1,2,3]triazol-1-yl]-piperidine-1-carboxylic acid tert-butyl ester | HCID 25176363 | — |
反応手順
4-Azido-piperidine-1-carboxylic acid text-butyl ester (1 eq) and 1-methanesulfonyl-4-prop-2-ynyloxy-benzene (1 eq) were suspended in H2O/t-BuOH (1:1). Sodium ascorbate (0.1 eq) was added followed by CuSO4.5H2O (0.01 eq). The mixture was stirred vigorously overnight. The mixture was diluted with water and a precipitate formed. The precipitate was collected by filtration and purified on silica gel to give the desired product. 1H NMR (CDCl3): δ 7.88 (2H, d), 7.67 (1H, s), 7.14 (2H, d), 5.29 (2H, s), 4.64 (1H, m), 4.28 92H, m), 3.05 (3H, s), 2.94 (2H, m), 2.2 (2H, m), 1.96 (2H, m), 1.48 (9H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08846675B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-038fb3f78e8e4754882901881e06898c |
| 出典メモ | uspto-grants-2014_09 |