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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31368생성일: 2026년 10월 24일

Triethylamine → [(S)-2-((S)-8-Azidomethyl-7,8-dihydro-[1,4]dioxino[2,3-g]indazol-1-yl)-1-methyl-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/31368

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium AzideHCID 33557—
반응물Methanesulfonic anhydrideHCID 81560—
반응물Sodium BicarbonateHCID 516892—
반응물[(S)-2-((S)-8-Hydroxymethyl-7,8-dihydro-[1,4]dioxino[2,3-g]indazol-1-yl)-1-methylethyl]-carbamic acid tert-butyl esterHCID 69252403—
용매Dimethyl SulfoxideHCID 679—
용매TetrahydrofuranHCID 8028—
생성물[(S)-2-((S)-8-Azidomethyl-7,8-dihydro-[1,4]dioxino[2,3-g]indazol-1-yl)-1-methyl-ethyl]-carbamic acid tert-butyl esterHCID 8660534189.5%

반응 조건

온도90 °C

반응 단계

To a 0° C. stirred solution of the alcohol from Step A (0.69 g, 1.87 mmol) in anhydrous tetrahydrofuran (30 mL) was added triethylamine (0.38 g, 0.52 mL, 3.7 mmol) and methanesulfonic anhydride (0.49 g, 2.81 mmol) under a nitrogen atmosphere. After 1 h the volatiles were evaporated. To the residue was added anhydrous DMSO (40 mL) and sodium azide (2.43 g, 37 mmol). The resulting mixture was heated at 90° C. for 1 h, cooled, mixed with a saturated aqueous solution of sodium bicarbonate (100 mL) and extracted with ethyl acetate (50 mL×3). Chromatography on silica eluting with a gradient of 0% to 25% ethyl acetate/hexane gave an oil (0.65 g, 88%), that solidified on standing. Crystallization from ethyl acetate/hexane gave a crystalline solid (0.48 g, 65%): mp 134-135° C. LCMS (+APCI) 395 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425572B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-085b03b4c67c420eb92635522fe99a89
출처 메모uspto-grants-2008_09