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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226281Generated: October 25, 2026

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/226281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-[4-((R)-2-hydroxy-2-phenylethylamino)phenyl]ethylamineHCID 10083753—
Reactant2-bromo-(R)-1-tert-butyldimethylsiloxy-1-(3-formamido-4-benzyloxyphenyl)ethaneHCID 57461067—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventIsopropyl AcetateHCID 7915—
ProductN-{2-[4-((R)-2-hydroxy-2-phenylethylamino)phenyl]ethyl}-(R)-2-tert-butyldimethylsiloxy-2-(3-formamido4-benzyloxyphenyl)ethylamineHCID 57755062100%

Reaction Conditions

Temperature140 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557247B2
Source datasetuspto-grants-2009_07
ORD IDord-19715f61058041ef894a38de7a6aaa62
Source noteuspto-grants-2009_07