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HRID 1947097作成日:2026年10月25日
Methanesulfonic acid, 1,1,1-trifluoro-, calcium salt (2:1) → trans-3-[4-(4-Chloro-phenyl)-[1,4]diazepan-1-yl]4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1947097
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanesulfonic acid, 1,1,1-trifluoro-, calcium salt (2:1) | HCID 2734307 | — |
| 反応物 | tert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylate | HCID 10103880 | — |
| 反応物 | 1-(4-Chlorophenyl)-1,4-diazepane | HCID 21363820 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | trans-3-[4-(4-Chloro-phenyl)-[1,4]diazepan-1-yl]4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 57982392 | 43.1% |
反応手順
To a solution of 1-(4-Chloro-phenyl)-[1,4]diazepane (1.00 g, 4.80 mmol) in acetonitrile (10 mL) was added 6-oxa-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester (0.925 g, 5.00 mmol) and calcium(II) trifluoromethanesulfonate (0.676 g, 2.00 mmol). The solution was stirred at 80° C. for 17 hours under nitrogen atmosphere. The reaction was concentrated in vacuo. The residue was diluted with saturated aqueous sodium bicarbonate (50 mL) and extracted with ethyl acetate (3×30 mL). The combined organics were washed with brine, dried over MgSO4, and evaporated. The residue was purified by silica gel chromatography (gradient ethyl acetate to 87:10:3 ethyl acetate:methanol:triethylamine) to yield 0.819 g (41%) of the title compound. ESI-MS m/z: 396 (M+1), FAS method rt: 1.25 min
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08399455B2 |
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| 出典データセット | uspto-grants-2013_03 |
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| ORD ID | ord-c74bfcfab9ba436a94f28b301b4ad790 |
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| 出典メモ | uspto-grants-2013_03 |
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