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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501996생성일: 2026년 10월 25일

Sodium Iodide → N-{2-[4-((R)-2-hydroxy-2-phenylethylamino)phenyl]ethyl}-(R)-2-tert-butyldimethylsiloxy-2-(3-formamido4-benzyloxyphenyl)ethylamine

https://huagongshe.com/reaction/501996

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물2-[4-((R)-2-hydroxy-2-phenylethylamino)phenyl]ethylamineHCID 10083753—
반응물2-bromo-(R)-1-tert-butyldimethylsiloxy-1-(3-formamido-4-benzyloxyphenyl)ethaneHCID 57461067—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매Isopropyl AcetateHCID 7915—
생성물N-{2-[4-((R)-2-hydroxy-2-phenylethylamino)phenyl]ethyl}-(R)-2-tert-butyldimethylsiloxy-2-(3-formamido4-benzyloxyphenyl)ethylamineHCID 57755062100%

반응 조건

온도140 °C

반응 단계

Intermediate 4 (5.0 g, 11 mmol), intermediate 2 (3.5 g, 14 mmol), and dimethylsulfoxide (10 mL) were combined in a 100 mL round bottom flask and stirred to form a homogeneous solution. Potassium carbonate (6.0 g, 43 mmol) and sodium iodide (1.7 g, 11 mmol) were added and the reaction mixture was heated to 140° C. The reaction mixture was maintained at 140° C. for 10 min, then cooled to room temperature and diluted with water (24 mL) and isopropyl acetate (28 mL). The reaction was stirred until all solids dissolved and then transferred to a separatory funnel. The organic layer was washed with water (17 mL) followed by acetate buffer (5% v/v acetic acid, 12% w/v sodium acetate trihydrate in water, 18 ml) followed by sodium bicarbonate solution (5% w/v in water, 17 mL) followed by saturated aqueous sodium chloride (17 mL). The organic layer was dried over sodium sulfate and concentrated to afford intermediate 5 as a brown gelatinous solid (7.0 g, 11 mmol, >99%). m/z: [M+H+] calcd for C38H49N3O4Si 640.4; found 640.6.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772434B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-e8f9814b472141e9ad3809f31ce54702
출처 메모uspto-grants-2010_08