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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816047Generated: November 1, 2026

2-Methylpropylenediamine → 5-[3-[(2-Amino-2-methylpropyl)amino]propyl]-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide, dihydrochloride salt

https://huagongshe.com/reaction/1816047

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpropylenediamineHCID 13128—
Reactantchloro-5-[3-[(methylsulfonyl)oxy]propyl]-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamideHCID 12988688—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-[3-[(2-Amino-2-methylpropyl)amino]propyl]-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide, dihydrochloride saltHCID 131724838—

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Methyl-1,2-propanediamine (0.12 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 (0.250 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 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 4M hydrochloric acid in dioxane gave the title compound as the dihydrochloride salt (0.045 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881754B2
Source datasetuspto-grants-2005_04
ORD IDord-a6d507a2aebe495fb17c2d522ca03173
Source noteuspto-grants-2005_04