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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2047076생성일: 2026년 10월 27일

1,1,3,3-Tetramethylguanidine → Ethyl 2-acetoxy-2-(4-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)cyclohexylidene)acetate

https://huagongshe.com/reaction/2047076

반응식

참여 물질

역할이름HCID투입량
반응물1,1,3,3-TetramethylguanidineHCID 66460—
반응물Lithium ChlorideHCID 433294—
반응물Ethyl 2-(acetyloxy)-2-(diethyl phosphono)acetateHCID 4131038—
반응물HCID 66583636HCID 66583636—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-acetoxy-2-(4-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)cyclohexylidene)acetateHCID 67494543—

반응 조건

온도-78 °C

반응 단계

To a 100 mL roundbottom flask was charged ethyl 2-acetoxy-2-(diethoxyphosphoryl)acetate (1121 mmol, 3.16 g), LiCl (11.21 mmol, 475 mg), and THF (25 mL). The flask was then flushed with argon, sealed, and cooled to −78° C. in a dry ice/IPA bath. Added dropwise to this solution was a solution of 1,1,3,3-tetramethylguanidine (11.21 mmol. 1.41 g) in THF (5 mL). The resulting solution was allowed to stir at −78° C. for 30 minutes. At 30 minutes, 4-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)cyclohexanone (5.09 mmol, 2.50 g) was added in THF (3 mL). The reaction was then allowed to slowly warm to room temperature and then stirred for 48 hours. After 48 hours, the reaction was diluted with DCM (100 mL) and washed with H2O (50 mL). The organic layer was collected, dried over Na2SO4, and reduced in vacuo. The resulting residue was purified via flash chromatography to yield the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08591943B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-645dd3294d7c41909f29b44c35b47f7c
출처 메모uspto-grants-2013_11