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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230183생성일: 2026년 10월 24일

Triethylamine → (R)-1-[6-Methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol

https://huagongshe.com/ko/reaction/230183

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(S)-(+)-1-Aminopropan-2-olHCID 7311736—
반응물4-Chloro-6-methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidineHCID 86600485—
용매TetrahydrofuranHCID 8028—
생성물(R)-1-[6-Methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-olHCID 68876938107.4%

반응 단계

4-Chloro-6-methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidine (391 mg, 1.182 mmol) was dissolved in 5 mL of dry THF. Triethylamine (239 mg, 2.363 mmol) was added, and the reaction mixture was stirred for four hours. (S)-1-Amino-propan-2-ol (93 mg, 1.241 mmol) was then added, and the reaction mixture was stirred for 64 hours. The reaction mixture was quenched by addition to water, and was partitioned between water and ethyl acetate. The organic layer was separated, dried over MgSO4, filtered, and evaporated under reduced pressure to give (R)-1-[6-Methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol (469 mg). Mass Spec. M+H=370.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566708B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-d86f1e23ab0341ae9b8e4a580b21a1cb
출처 메모uspto-grants-2009_07