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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16435생성일: 2026년 10월 24일

Diisopropylethylamine → 4-[(4aR,7aR)-Octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-6-({4-[(3-amino-1,2-benz-isoxazol-4-yl)oxy]-3-fluorophenyl}amino)-2-pyrimidinylamine

https://huagongshe.com/ko/reaction/16435

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(4aR,7aR)-Octahydro-1H-pyrrolo(3,4-b)pyridineHCID 1515156—
반응물N-{4-[(3-Amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}-N-(2-amino-6-chloro-4-pyrimidinyl)amineHCID 17979320—
용매2-EthylhexanolHCID 7720—
생성물4-[(4aR,7aR)-Octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-6-({4-[(3-amino-1,2-benz-isoxazol-4-yl)oxy]-3-fluorophenyl}amino)-2-pyrimidinylamineHCID 68426920—

반응 조건

온도150 °C

반응 단계

88 mg (0.23 mmol) of N-{4-[(3-amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}-N-(2-amino-6-chloro-4-pyrimidinyl)amine (from example 3) and 114.8 mg (0.91 mmol) of [(4aR,7aR)-octahydro-6H-pyrrolo[3,4-b]pyridine together with 294.1 mg (2.28 mmol) of diisopropylethylamine are dissolved in 4 ml of 2-ethylhexanol, and the mixture is stirred at 150° C. for 3 h. After cooling, the reaction mixture is filtered and water is added. The mixture is extracted repeatedly with ethyl acetate, the organic phase is dried over magnesium sulfate and the solvent is removed under reduced pressure. The residue is purified by preparative HPLC.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737153B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-30b698dcf3db4e6b9e7782296266353a
출처 메모uspto-grants-2010_06