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HRID 988748생성일: 2026년 10월 26일

Hydrochloric Acid → (S)-2-methyl-3-quinoxalin-6-yl-propan-1-ol

https://huagongshe.com/reaction/988748

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ammonium HydroxideHCID 14923—
반응물1,4-Dioxane-2,3-diolHCID 96170—
반응물(S)-3-Benzo[1,2,5]thiadiazol-5-yl-2-methyl-propan-1-olHCID 69711262—
촉매ZincHCID 23994—
용매EthanolHCID 702—
생성물(S)-2-methyl-3-quinoxalin-6-yl-propan-1-olHCID 69709252—

반응 단계

A solution of (S)-3-benzo[1,2,5]thiadiazol-5-yl-2-methyl-propan-1-ol (5 g, 24 mmol) in EtOH (60 ml) is cooled to 0° and then treated with half concentrated HCl (40 ml, ca. 200 mmol). Zn dust (8.5 g, 130 mmol) is added in 1 g portions at 0°, one portion every 5 minutes. After the last addition, the mixture is stirred at 10° to 15° for 45 minutes. Under ice cooling, half concentrated NH4OH (40 ml, ca. 290 mmol) is added dropwise. The mixture is filtered over Hyflo, the filtrate concentrated under reduced pressure and the remaining aqueous phase twice extracted with EtOAc (150 ml, 50 ml). Drying over Na2SO4 and evaporation give the diamnino intermediate as a brownish, clear oil which tends to darken upon exposure to light and air. This intermediate is dissolved in absolute EtOH (60 ml) and cooled to 0°. 1,4dioxane-2,3-diol (3.75 g, 31.2 mmol) is added at once and the solution stirred at room temperature for 2 h. The mixture is evaporated to dryness, the residue distributed between brine (50 ml) and DCM (50 ml), the organic phase washed with brine (25 ml), dried over Na2SO4 and evaporated to afford (S)-2-methyl-3-quinoxalin-6-yl-propan-1-ol as a brownish, clear, viscous oil of sufficient purity for the next step. ee=91% (HPLC on chiral stat. phase). TLC (silicagel, DCM/MeOH/NH4OH 85:15:1): rf 0.68.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06635647B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-fb41a96189114d17bb8fc64b06a3c4d0
출처 메모uspto-grants-2003_10