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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183043Generated: November 2, 2026

1,3-Propanediamine, N1,N1,N3-trimethyl- → HCID 59909772, compound

https://huagongshe.com/reaction/2183043

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N1,N1,N3-trimethyl-HCID 78302—
Reactantethyl 5-{(1R)-1-[2-(tert-butoxy)-2-oxoethyl]4-cyclohexylbutyl}-1,2,4-oxadiazole-3-carboxylateHCID 59909797—
SolventEthanolHCID 702—
ProductHCID 59909772HCID 5990977278.7%

Reaction Conditions

Temperature85 °C

Reaction Steps

A solution of ethyl 5-{(1R)-1-[2-(tert-butoxy)-2-oxoethyl]-4-cyclohexylbutyl}-1,2,4-oxadiazole-3-carboxylate (Preparation 3) (550 mg, 1.40 mmol) in ethanol (2 ml) was treated with N,N,N′-trimethyl-1,3-propanediamine (1.02 ml, 7.00 mmol) and the resulting mixture was heated at 85° C. in a sealed tube for 3 hours. The solvent removed under reduced pressure. The residue was purified by column chromatography on silica eluting with a gradient system of 97:3:0.3 (dichloromethane:methanol:ammonia) gradually changing to 90:10:1 (dichloromethane:methanol:ammonia) to afford the title compound as a colourless oil (512 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897306B2
Source datasetuspto-grants-2005_05
ORD IDord-ec93a86167874cfe913205617747af35
Source noteuspto-grants-2005_05