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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1958377생성일: 2026년 10월 27일

2-Ethyl-1-butanol → 4-[1-(4-Methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidine-1-carboxylic acid 2-ethyl-butyl ester

https://huagongshe.com/reaction/1958377

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethyl-1-butanolHCID 7358—
반응물TriethylamineHCID 8471—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물1-(4-methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidineHCID 11360802—
용매Dimethyl SulfoxideHCID 679—
생성물4-[1-(4-Methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidine-1-carboxylic acid 2-ethyl-butyl esterHCID 2189770344.6%

반응 단계

Di-imidazol-1-yl-methanone (0.51 mmol, 83 mg), and 2-ethyl-butan-1-ol (0.51 mmol, 52 mg) were dissolved in DMSO (1 mL) and stirred for 30 minutes at room temperature. Then, 1-(4-methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine (0.17 mmol, 70 mg) and triethylamine (0.51 mmol, 72 μL) were added and heated in a microwave at 120° C. for 6 minutes. The progress of the reaction was monitored by LCMS. The reaction mixture was quenched with water and the product was extracted with ethylacetate. Removal of organic solvents in vacuo and purification by HPLC provided Compound A119 as a white solid (38 mg, 36%). Exact mass calculated for C24H31N5O5S 501.60, found 502.3 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410119B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-87049137b82b48588d3395c2fd9dcb60
출처 메모uspto-grants-2013_04