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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593816Generated: October 31, 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/1593816

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 suflate and concentrated under reduced pressure. Purification by preperative 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 4 M hydrochloric acid in dioxane gave the title compound as the dihydrochloride salt (0.045 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297818B2
Source datasetuspto-grants-2007_11
ORD IDord-dc1bc142732d4b3e9774529ddf45cca5
Source noteuspto-grants-2007_11