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HRID 1828337생성일: 2026년 10월 25일

Ethyl Acetate → (R)-3-t-butyloxycarbonylamino-1-carbomethoxymethyl-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1828337

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Methyl bromoacetateHCID 60984—
반응물Sodium MethoxideHCID 10942334—
반응물(R)-3-t-butyloxycarbonylamino-3,4-dihydrocarbostyrilHCID 69198597—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(R)-3-t-butyloxycarbonylamino-1-carbomethoxymethyl-3,4-dihydrocarbostyrilHCID 6919487272.4%

반응 단계

(R)-3-t-butyloxycarbonylamino-3,4-dihydrocarbostyril (26 mg), as prepared in Example 5, was dissolved in tetrahydrofuran (5 mL) at room temperature under argon. To the stirring solution was added methyl bromoacetate (31 mg), followed by sodium methoxide (26 mg). The resulting suspension was stirred for 30 min before dilution with ethyl acetate (25 mL) and water (25 mL). The organic phase was separated, washed with water (25 mL), and dried over anhydrous sodium sulfate. After solvent evaporation under vacuum, the crude product was purified by reverse phase preparative HPLC to provide (R)-3-t-butyloxycarbonylamino-1-carbomethoxymethyl-3,4-dihydrocarbostyril (24 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07057046B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-577c729936e1488d86acc2ce35c04ab7
출처 메모uspto-grants-2006_06