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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108401Generated: October 25, 2026

Ammonium Chloride → HCID 70234416, compound

https://huagongshe.com/reaction/1108401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(+)-BenzylphenethylamineHCID 1268086—
Reactant3-(6-Amino-pyridin-3-yl)-acrylic acid tert-butyl esterHCID 53665462—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70234416HCID 70234416—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of (R)-(+)-N-benzyl-α-methylbenzylamine (4.0 g, 19 mmol) in 50 mL THF was gradually added n-butyllithium (11.3 mL, 2.5 M, 28.2 mmol) over 5 min. The mixture was stirred for 30 min at 0° C. and cooled to -78° C. A solution of 10-2 (2.0 g, 9.4 mmol) in 20 mL THF was gradually added. After stirring for 40 min at -78° C., it was treated with NH4Cl (sat.) at -78° C., warmed to room temperature and extracted three times with EtOAc. The combined organic layers were washed with brine and dried over Na2SO4. After solvent evaporation, the residue was purified using silica gel flash chromatography (EtOAc/hexanes 1:2) to afford the desired product 10-3 as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066648
Source datasetuspto-grants-2000_05
ORD IDord-f565a98a33394e01a7d3e9e484a4451c
Source noteuspto-grants-2000_05