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HRID 564219作成日:2026年10月27日

Ammonium Hydroxide → (R)-tert-butyl 2-(5-methoxycarbonylthiophen-2-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/564219

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物Methyl 5-bromothiophene-2-carboxylateHCID 605713—
反応物N-Boc-pyrrolidineHCID 643455—
反応物SparteineHCID 644020—
反応物Tri-t-butylphosphine fluoroborateHCID 44558591—
反応物CID 53628100HCID 178418400—
触媒palladium(II) acetateHCID 167845—
触媒ZincchlorideHCID 3007855—
溶媒Diethyl EtherHCID 3283—
溶媒CyclohexaneHCID 8078—
溶媒tert-Butyl methyl etherHCID 15413—
生成物(R)-tert-butyl 2-(5-methoxycarbonylthiophen-2-yl)pyrrolidine-1-carboxylateHCID 66758892—

反応手順

To a solution of N-Boc-pyrrolidine (3 mL) and (−)-sparteine (3.9 mL) in tert-butyl methyl ether (36 mL) at −78° C. was added 1.4M sec-butyl lithium in cyclohexane (12.21 mL). The solution was stirred for 3 hours and 1M zinc chloride in ether (10.2 mL) was added. The mixture was stirred for 30 minutes and warmed to ambient temperature for 30 minutes. Methyl 5-bromothiophene-2-carboxylate (3.15 g), tri-tert-butylphosphine tetrafluoroborate (249 mg) and palladium(II) acetate (153 mg) were added, and the mixture was stirred at ambient temperature overnight, treated with concentrated ammonium hydroxide (1 mL) and stirred for 30 minutes, and filtered through diatomaceous earth (Celite®). The filtrate was washed with 0.5M hydrochloric acid solution and water and concentrated. The concentrate was flash chromatographed on silica gel with ethyl acetate/hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067613B2
出典データセットuspto-grants-2011_11
ORD IDord-6c310ccc24894e758f571d8f23d9781f
出典メモuspto-grants-2011_11