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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11576생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/11576

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 번호US07098235B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d12725ce188849a28139487c1b120a88
출처 메모uspto-grants-2006_08