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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 467587생성일: 2026년 10월 25일

Triethylamine → HCID 178480679, 화합물

https://huagongshe.com/reaction/467587

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물2-Chloro-6-fluoroanilineHCID 2734205—
반응물6,6-Dimethyl-3-[4-(4-methyl-piperazin-1-yl)-benzoylamino]-5,6-dihydro-4H-pyrrolo[3,4-c]pyrazole-2-carboxylic acid ethyl ester dihydrochlorideHCID 67237574—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물HCID 178480679HCID 1784806796%

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온도50 °C

반응 단계

To a solution of di-tert-butyl dicarbonate (101 mg, 0.46 mmol, 1.1 eq) in DCM (2 mL) was added 2-chloro-6-fluoroaniline (61 mg, 0.42 mmol, 1 eq) and N,N-dimethylpyridin-4-amine (51 mg, 0.42 mmol, 1 eq). After 1 hour of agitation at room temperature, 6,6-Dimethyl-3-[4-(4-methyl-piperazin-1-yl)-benzoylamino]-5,6-dihydro-4Hpyrrolo[3,4-c]pyrazole-2-carboxylic acid ethyl ester dihydrochloride (189 mg, 0.38 mmol, 0.9 eq), triethylamine (0.23 mL, 1.68 mmol, 4 eq) and an additional 2 mL of DCM (4 mL total). The cocktail was placed in a Personal Chemistry, Smith Creator microwave reaction station and the vial contents were irradiated at 125° C. for 10 minutes with application of continuous, simultaneous cooling. After the 10 minutes of heating time had elapsed, the solution was washed twice with water. The organic phase was collected and the solvent was removed in vacuo. The residue was dissolved in methanol (3 mL), treated with triethylamine (0.3 mL, 2.2 mmol, 5 eq) and agitated for 6 hours at 50° C. After evaporation of the solvent, the solid was purified by preparative HPLC to afford 0.012 g of the title compound in 5% overall yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623876B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-151144188a5e4adaaa0764b86c3dce99
출처 메모uspto-grants-2014_01