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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 449755생성일: 2026년 10월 24일

2,5-Dimethoxytetrahydrofuran → (S)-methyl 6-benzyloxycarbonylamino-2-carbazol-9-yl-hexanoate

https://huagongshe.com/ko/reaction/449755

반응식

참여 물질

역할이름HCID투입량
반응물2,5-DimethoxytetrahydrofuranHCID 79098—
반응물methyl (2S)-2-amino-6-(phenylmethoxycarbonylamino)hexanoateHCID 6994982—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물(S)-methyl 6-benzyloxycarbonylamino-2-carbazol-9-yl-hexanoateHCID 6799316649.5%

반응 조건

온도110 °C

반응 단계

A vigorously stiffed solution of L-Lys(Z)—OMe (3.31 g, 10 mmol) in acetic acid (20 mL) and dioxane (40 mL) was heated to 75° C., at this temperature 2,5-dimethoxytetrahydrofuran (DMTHF, ee 97%) (3.97 g, 3.90 mL, 30 mmol) was added dropwise to the reaction mixture. After complete addition of DMTHF, the reaction mixture was refluxed at 110° C. for 3 h followed by 5-6 h stiffing at room temperature. The volatiles were removed under reduced pressure to afford a dark brown residue, which was dissolved in dichloromethane (100 mL) and washed with 10% NaHCO3 solution (15 mL), brine (15 mL) and water (15 mL). The organic phase was dried over anhydrous Na2SO4 and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (230-400 mesh) using hexane:ethyl acetate (7:3) as eluent to afford (S)-methyl 6-benzyloxycarbonylamino-2-carbazol-9-yl-hexanoate 3 (1.10 g, 25%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486534B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-6d9649b7421447f4a7a6b7819e714072
출처 메모uspto-grants-2013_07