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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tri-tert-butyl 1,4,7,10-Tetraazacyclododecane-1,4,7-triacetate | HCID 11237632 | — |
| Reactant | 2-Chloro-N-(4-tert-butylphenylmethyl)-acetamide | HCID 46837194 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,4,7-Tris(tert-butoxycarbonylmethyl)-10-((4-tert-butyl)-benzylaminocarbonylmethyl)-1,4,7,10-tetraazacyclodo-decane | HCID 68636242 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273874B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-65efecc08c5443e98dc9583fadb6e478 |
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| Source note | uspto-grants-2012_09 |
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