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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 719462생성일: 2026년 10월 26일

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/719462

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 번호US07132426B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-e0be510e98a54e598d8b6de37f65b688
출처 메모uspto-grants-2006_11