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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532327Generated: October 31, 2026

Phenylethanolamine → 5-(N-(2-Hydroxy-2-phenylethyl)-2-aminoethyl)amino-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide

https://huagongshe.com/reaction/1532327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylethanolamineHCID 1000—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-5-(2-chloroethyl)amino-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)benzamideHCID 11417653—
SolventTetrahydrofuranHCID 8028—
Product5-(N-(2-Hydroxy-2-phenylethyl)-2-aminoethyl)amino-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamideHCID 2067003734.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Chloro-5-(2-chloroethyl)amino-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)benzamide from Example 63 (0.1 g), 2-amino-1-phenylethanol (0.539 g) and triethylamine (0.5 ml) were dissolved in tetrahydrofuran (3 ml) and heated at 80° C. for 60 hours in a sealed tube. The reaction mixture was concentrated under reduced pressure, the residue was suspended in aqueous sodium hydrogen carbonate (30 ml), the product was extracted into ethyl acetate (3×30 ml), dried over magnesium sulphate filtered and concentrated under reduced pressure. Purification by NPHPLC eluting with 0 to 25% ethanol in dichloromethane gave title compound as a white solid (0.044 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06201024B1
Source datasetuspto-grants-2001_03
ORD IDord-b9cd7a06e44e46adb1dd6f4bc6ee9eda
Source noteuspto-grants-2001_03