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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390752Generated: October 26, 2026

Potassium Carbonate → 1,4,7-Tris(tert-butoxycarbonylmethyl)-10-((4-tert-butyl)-benzylaminocarbonylmethyl)-1,4,7,10-tetraazacyclodo-decane

https://huagongshe.com/reaction/2390752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-tert-butyl 1,4,7,10-Tetraazacyclododecane-1,4,7-triacetateHCID 11237632—
Reactant2-Chloro-N-(4-tert-butylphenylmethyl)-acetamideHCID 46837194—
SolventAcetonitrileHCID 6342—
Product1,4,7-Tris(tert-butoxycarbonylmethyl)-10-((4-tert-butyl)-benzylaminocarbonylmethyl)-1,4,7,10-tetraazacyclodo-decaneHCID 68636242—

Reaction Conditions

Temperature75 °C

Reaction Steps

A reaction mixture of 1,4,7-tris(tert-butoxycarbonylmethyl)-1,4,7,10-tetraaza-cyclododecane (7.57 g, 12.7 mmol), 2-chloro-N-(4-tert-butylphenylmethyl)-acetamide (3.60 g, 15 mmol) obtained from Example 2a and potassium carbonate (5.53 g, 40 mmol) in acetonitrile (100 ml) was heated to 75° C. and stirred under nitrogen-atmosphere overnight. The reaction mixture was cooled to room temperature and filtered. The filtrate was evaporated in vacuo and the residue was submitted to flash-chromatography (silica, MeOH/CHCl3). The fractions containing the product were combined and evaporated in vacuo resulting in the title compound being a yellow oil that crystallised upon storage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273874B2
Source datasetuspto-grants-2012_09
ORD IDord-65efecc08c5443e98dc9583fadb6e478
Source noteuspto-grants-2012_09