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HRID 79689作成日:2026年10月24日

Glycine tert-butyl ester → 5-[(Tert-butoxycarbonylmethyl-amino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

https://huagongshe.com/ja/reaction/79689

反応式

関与物質

役割名称HCID仕込み量
反応物Glycine tert-butyl esterHCID 151417—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物5-Formyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl esterHCID 72338046—
溶媒DichloromethaneHCID 6344—
生成物5-[(Tert-butoxycarbonylmethyl-amino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl esterHCID 6662093047.1%

反応手順

Sodium triacetoxyborohydride (2.08 g, 9.86 mmol) was added to a solution of 5-formyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (891 mg, 3.29 mmol) and glycine t-butyl ester (1.65 g, 9.86 mmol) in dichloromethane (20 mL) over 2 minutes—a small amount of gas evolution was observed. After 1 hour the reaction was quenched with saturated ammonium chloride (5 mL). The mixture was extracted with ethyl acetate (3×25 mL). The combined organic phases were dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The resulting residue was purified by flash chromatography with methanol and dichloromethane as the eluant at a gradient of 0-10%. The fractions containing product were combined and the solvent was removed under reduced pressure to provide 5-[(tert-butoxycarbonylmethyl-amino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (601 mg, 1.55 mmol, 47%). C19H34N2O6 calculated 386.2, observed [M+1]+ 387.2; rt=1.61 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841278B2
出典データセットuspto-grants-2014_09
ORD IDord-009df566ff8b442cbc8d90e62599bb72
出典メモuspto-grants-2014_09