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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 628955생성일: 2026년 10월 26일

Toluene → HCID 52935026, 화합물

https://huagongshe.com/reaction/628955

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물1-(2-Methoxyethyl)-1H-pyrazole-4-boronic acid, pinacol esterHCID 11230491—
반응물1-Methylethyl((cis)-1-acetyl-6-bromo-2-methyl-1,2,3,4-tetrahydro-4-quinolinyl)carbamateHCID 52935020—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
생성물HCID 52935026HCID 52935026—

반응 단계

1-Methylethyl [(2S,4R)-1-acetyl-6-bromo-2-methyl-1,2,3,4-tetrahydro-4-quinolinyl]carbamate (for preparation see Intermediate 1) (185 mg), 1-[2-(methyloxy)ethyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (for a preparation see Journal of Heterocyclic Chemistry, 41(6), 931-939; 2004) (151 mg), potassium carbonate (90 mg) and tetrakis(triphenylphosphine)palladium(0) (28.9 mg) were combined in ethanol and toluene under nitrogen and heated to 80° C. for 18 h. The reaction was concentrated, the residue partioned between ethyl acetate (10 ml) and water (10 ml) and the aqueous layer was extracted with ethyl acetate (10 ml). The combined organics were washed with brine (25 ml), dried with sodium sulphate, filtered and concentrated. The residue was purified by MDAP (formate ×2) and the collected product dissolved in 1,4-dioxane (0.5 ml) and cooled in a CO2 bath then left on a freeze dryer overnight. The resulting white solid was dried at 40° C. under vacuum overnight to give 1-methylethyl ((2S,4R)-1-acetyl-2-methyl-6-{1-[2-(methyloxy)ethyl]-1H-pyrazol-4-yl}-1,2,3,4-tetrahydro-4-quinolinyl)carbamate (84.7 mg). LCMS (formate), Rt 0.84 min, MH+ 415

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315487B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-9ad27da81bac46b78e4f45c19a0da560
출처 메모uspto-grants-2016_04