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HRID 225964作成日:2026年10月27日

Triethylamine → methyl [(2S,4EZ)-1-(biphenyl-4-yl-carbonyl)--4-(methoxyimino)pyrrolidin-2-yl]acetate

https://huagongshe.com/reaction/225964

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物O-methylhydroxylammonium chlorideHCID 11639—
反応物methyl [(2S)-1-(biphenyl-4-ylcarbonyl)-4-oxopyrrolidin-2-yl]acetateHCID 86760911—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物methyl [(2S,4EZ)-1-(biphenyl-4-yl-carbonyl)--4-(methoxyimino)pyrrolidin-2-yl]acetateHCID 13172752684%

反応手順

A solution of methyl [(2S)-1-(biphenyl-4-ylcarbonyl)-4-oxopyrrolidin-2-yl]acetate (43 mg, 0.13 mmol), hydroxylamine methyl ether hydrochloride (32 mg, 0.38 mmol) and triethylamine (53 μl, 0.38 mmol) in chloroforme (3 ml) was stirred at 70° C. for 5 days. The reaction mixture was diluted with dichloromethane and washed with HCl 1N. The organic phase was dried (MgSO4) and concentrated to afford methyl [(2S,4EZ)-1-(biphenyl-4-yl-carbonyl)--4-(methoxyimino)pyrrolidin-2-yl]acetate (40 mg). Yield: 62%. HPLC purity: 94%

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557136B2
出典データセットuspto-grants-2009_07
ORD IDord-fd74bb2257964a56a4a9068902b53e9a
出典メモuspto-grants-2009_07