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HRID 277785作成日:2026年10月25日

(2R)-Oxiran-2-ylmethyl butanoate → HCID 54330421、化合物

https://huagongshe.com/reaction/277785

反応式

関与物質

役割名称HCID仕込み量
反応物(2R)-Oxiran-2-ylmethyl butanoateHCID 2724536—
反応物3,6-Dihydro-4-[4-[[(phenylmethoxy)carbonyl]amino]phenyl]-1(2H)-pyridinecarboxylic acid phenylmethyl esterHCID 54271798—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 54330421HCID 54330421—

反応条件

温度-78 °C

反応手順

A solution of 3,6-dihydro-4-[4-[[(phenylmethoxy)carbonyl]amino]phenyl]-1(2H)-pyridinecarboxylic acid phenylmethyl ester (EXAMPLE 17, Step 2, 0.500 g) in dry tetrahydrofuran (5.7 mL) at −78° C. under N2 is treated with n-butyllithium (0.73 mL, 1.6M in hexanes) dropwise over five minutes. The resulting mixture is stirred at −78° C. for 45 minutes and is then treated with (R)-(−)-glycidyl butyrate dropwise. The resulting solution is allowed to warm to ambient temperature over approximately 45 minutes and is stirred for an additional 20 hours, after which the reaction is quenched with saturated aqueous ammonium chloride (10 mL), diluted with water (20 mL) and extracted with ethyl acetate (2×15 mL). The combined organic phase is washed with saline (10 mL), dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the crude product which is chromatographed on silica gel (230-400 mesh, 40 g), eluting with methanol/methylene chloride (1/99). Pooling and concentration of those fractions with an Rf=0.37 by TLC (methanol/chloroform, 5/95) gives the title compound, mp 131.5-133.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358942B1
出典データセットuspto-grants-2002_03
ORD IDord-42ee1b32a40943088d2cca5fa55b4207
出典メモuspto-grants-2002_03