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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719625Generated: October 26, 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/719625

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 numberUS07132457B2
Source datasetuspto-grants-2006_11
ORD IDord-8718d5a4dd114ac298310ca5d6f8c679
Source noteuspto-grants-2006_11