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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816048Generated: November 1, 2026

4-Amino-1-butanol → 2-Chloro-5-[3-[(4-hydroxybutyl)amino]propyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide

https://huagongshe.com/reaction/1816048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-butanolHCID 25868—
Reactantchloro-5-[3-[(methylsulfonyl)oxy]propyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamideHCID 12988688—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-5-[3-[(4-hydroxybutyl)amino]propyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamideHCID 10224786—

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Amino-1-butanol (0.11 ml) was added to a solution of 2-chloro-5-[3-[(methylsulfonyl)oxy]propyl)-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide (0.25 g, Example 6e) in tetrahydrofuran (4 ml) and heated at 60° C. in a sealed tube for 12 h. On cooling to ambient temperature, the mixture was diluted with ethyl acetate and extracted twice with saturated aqueous sodium hydrogencarbonate solution and once with brine, dried over magnesium sulfate and concentrated under reduced pressure. Purification by preparative reverse phase HPLC (eluting with a gradient of acetonitrile in 0.1% aqueous ammonium acetate/25-95%) gave the title compound as the acetate salt. Treatment with aqueous 2M sodium hydroxide and extraction into ethyl acetate gave the title compound (0.065 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881754B2
Source datasetuspto-grants-2005_04
ORD IDord-eee4996b05fd41638dead36d9d287371
Source noteuspto-grants-2005_04