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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816035Generated: November 2, 2026

Water → 2-Chloro-5-[[2-(2-hydroxyethoxy)ethylamino]methyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide

https://huagongshe.com/reaction/1816035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiglycolamineHCID 13578—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Chloro-5-formyl-N-(tricyclo [3.3.1.13,7]dec-1-ylmethyl)-benzamideHCID 12085346—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product2-Chloro-5-[[2-(2-hydroxyethoxy)ethylamino]methyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamideHCID 10223937—

Reaction Steps

To a solution of 2-chloro-5-formyl-N-(tricyclo [3.3.1.13,7] dec-1-ylmethyl)-benzamide (0.150 g, Example 1b) and 2-(2-aminoethoxy)ethanol (0.065 ml) in 1,2-dichloroethane (6 ml) was added sodium triacetoxyborohydride (0.134 g), and the mixture was stirred overnight at room temperature. Water (20 ml) and dichloromethane (20 ml) were added and the layers were partitioned. The organics were washed with brine (30 ml), dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by NPHPLC eluting with a gradient of 0-10% ethanol in dichloromethane to give the title compound as a white powder (0.016 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881754B2
Source datasetuspto-grants-2005_04
ORD IDord-b643c1597b26494fa80ac6eb40ab3be6
Source noteuspto-grants-2005_04