関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Benzoic acid, 3-(chlorosulfonyl)-, methyl ester | HCID 113339 | — |
| 反応物 | Tert-butyl 3-aminopropanoate hydrochloride | HCID 16218890 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 3-(2-tert-Butoxycarbonyl-ethylsulfamoyl)-benzoic acid methyl ester | HCID 66797835 | — |
反応手順
To a stirred solution of methyl 3-(chlorosulfonyl)benzoate (5.0 g, 21.31 mmol) in pyridine (50 ml), was added dropwise a solution of tert-butyl 3-aminopropanoate hydrochloride (5.11 g, 23.44 mmol) in pyridine (10 ml) at 0° C. The resulting solution was allowed to warm to RT and stirred for 4 h. 1N HCl (50 ml) was added to the reaction mixture and the aqueous phase was separated and extracted with DCM (3×20 ml). The combined organic fractions were dried (MgSO4) and concentrated in vacuo to afford a viscous amber oil. Purification by chromatography on silica eluting with 0-100% EtOAc in iso-hexane afforded the title compound as a colourless oil. 1H NMR (400 MHz, CDCl3) δ 8.53 (1H, s), 8.27 (1H, d), 8.08 (1H, d), 7.63 (1H, t) 5.38 (1H, t), 3.97 (3H, s), 3.20 (2H, m), 2.48 (2H, t), 1.43 (9H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08372845B2 |
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| 出典データセット | uspto-grants-2013_02 |
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| ORD ID | ord-fa88b3d719684d9c8ce61b0904b53a87 |
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| 出典メモ | uspto-grants-2013_02 |
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