Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719634Generated: October 30, 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/719634

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 numberUS07132457B2
Source datasetuspto-grants-2006_11
ORD IDord-d1e12b11ac884db794e379a2cb74e585
Source noteuspto-grants-2006_11