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HRID 588317作成日:2026年10月26日
18-Crown-6 → (r)-5-Biphenyl-4-ylmethyl-3-[1-diisopropylamino-meth-(e)-ylidene]-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/588317
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 18-Crown-6 | HCID 28557 | — |
| 反応物 | N,N,N',N',N'',N''-Hexamethylmethanetriamine | HCID 79831 | — |
| 反応物 | tert-Butoxy bis(dimethylamino)methane | HCID 79885 | — |
| 反応物 | 1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine | HCID 547712 | — |
| 反応物 | Potassium hexafluorophosphate | HCID 23688904 | — |
| 反応物 | (S)-2-biphenyl-4-ylmethyl-5-oxopyrrolidine-1-carboxylic acid t-butyl ester | HCID 46193436 | — |
| 生成物 | (r)-5-Biphenyl-4-ylmethyl-3-[1-diisopropylamino-meth-(e)-ylidene]-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 58160400 | — |
反応手順
(S)-2-Biphenyl-4-ylmethyl-5-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester (8-a, R1=Boc) (2 mmol) is added to potassium hexafluorophosphate (1 eq) and 18-crown-6 (1 eq). Bredereck's reagent [Tris(dimethylamino)methane (13, R6=Me, R7=Me), Tert-Butoxy-bis(dimethylamino)methane (14, R6=Me, R7=Me, R8=tBu) and N,N-Dimethylformamide di-tert-butyl acetal (15, R6=Me, R7=Me, R8=tBu)] (4 ml) is added. The mixture is then stirred at ambient temperature for 3 h to afford (R)-5-biphenyl-4-ylmethyl-3-[1-dimethylaminometh-(E/Z)-ylidene]-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester (7-a, R1=Boc, R6=Me, R7=Me) or a salt thereof. The solutions are analysed by TLC (50% ethyl acetate in hexane). RF 0.21 (salt of 7-a, R1=Boc, R6=Me, R7=Me); RF 0.27 (7-a, R1=Boc, R6=Me, R7=Me); RF 0.68 (8-a, R1=Boc).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09227934B2 |
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| 出典データセット | uspto-grants-2016_01 |
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| ORD ID | ord-3a395fe4c13a4c67b7d574e24515cd9c |
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| 出典メモ | uspto-grants-2016_01 |
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