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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

反応式

関与物質

役割名称HCID仕込み量
反応物18-Crown-6HCID 28557—
反応物N,N,N',N',N'',N''-HexamethylmethanetriamineHCID 79831—
反応物tert-Butoxy bis(dimethylamino)methaneHCID 79885—
反応物1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
反応物Potassium hexafluorophosphateHCID 23688904—
反応物(S)-2-biphenyl-4-ylmethyl-5-oxopyrrolidine-1-carboxylic acid t-butyl esterHCID 46193436—
生成物(r)-5-Biphenyl-4-ylmethyl-3-[1-diisopropylamino-meth-(e)-ylidene]-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09227934B2
出典データセットuspto-grants-2016_01
ORD IDord-3a395fe4c13a4c67b7d574e24515cd9c
出典メモuspto-grants-2016_01