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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1864108생성일: 2026년 10월 27일

Triethylamine → 4-[1-(4-Methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidine-1-carboxylic acid 2,2-dimethyl-propyl ester

https://huagongshe.com/reaction/1864108

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,2-Dimethylpropyl carbonochloridateHCID 3352185—
반응물1-(4-Methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine hydrochlorideHCID 21897774—
용매DimethylformamideHCID 6228—
생성물4-[1-(4-Methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidine-1-carboxylic acid 2,2-dimethyl-propyl esterHCID 2189767533.8%

반응 단계

1-(4-Methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine hydrochloride (0.17 mmol, 70 mg), neopentyl chloroformate (0.25 mmol, 37 μL) and triethylamine (0.51 mmol, 72 μL) were dissolved in DMF (2 mL) and stirred for 60 minutes at room temperature. Progress of the reaction was monitored by TLC and LCMS. The reaction mixture was quenched with water. The product was extracted with ethyl acetate. Removal of organic solvents in vacuo and purification by HPLC provided Compound A124 as a white solid (28 mg, 27%). Exact mass calculated for C23H29N5O5S 487.57, found 488.20 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07625906B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-4b8f6a5d43954889b220191eaa6221fc
출처 메모uspto-grants-2009_12