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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 881518생성일: 2026년 10월 27일

Acetic Acid → 2-(4-((2-Chloro-4-morpholinothieno[2,3-d]pyrimidin-6-yl)methyl)piperazin-1-yl)ethanol

https://huagongshe.com/reaction/881518

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1-(2-Hydroxyethyl)piperazineHCID 7677—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-Chloro-4-morpholinothieno[2,3-d]pyrimidine-6-carbaldehydeHCID 56833844—
용매1,2-DichloroethaneHCID 11—
생성물2-(4-((2-Chloro-4-morpholinothieno[2,3-d]pyrimidin-6-yl)methyl)piperazin-1-yl)ethanolHCID 5823399251.5%

반응 단계

To a solution of 2-chloro-4-morpholinothieno[2,3-d]pyrimidine-6-carbaldehyde (1.1 g, 3.9 mmol) in 1,2-dichloroethane (20 mL) was added 1-(2-hydroxyethyl)piperazine (0.7 mL, 5.4 mmol), and AcOH (3.9 mmol). After the reaction mixture stirred 10 min at room temperature, Na(OAc)3BH (4.6 mmol) was added then the mixture stirred 72 h at room temperature. The reaction was quenched by the addition of saturated aqueous NaHCO3. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined organics were dried over Na2SO4 and concentrated in vacuo. 2-(4-((2-chloro-4-morpholinothieno[2,3-d]pyrimidin-6-yl)methyl)piperazin-1-yl)ethanol was purified by silica gel chromatography (0-20% MeOH in CH2Cl2) to afford 2-(4-((2-chloro-4-morpholinothieno[2,3-d]pyrimidin-6-yl)methyl)piperazin-1-yl)ethanol (0.8 g). MS (Q1) 398 (M)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08993563B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-6ce15311d4f94a288a56c9969b360435
출처 메모uspto-grants-2015_03