Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N,N′-1,2-Ethanediylbis[4-methyl-N-[3-[[(4-methylphenyl)sulfonyl]amino]propyl]benzenesulfonamide] | HCID 3090848 | — |
| Product | HCID 86667390 | HCID 86667390 | — |
Reaction Steps
Subsequently, 126 g (0.16 mol) of 1,5,8,12-Tetrakis(p-tolylsulfonyl)-1,5,8,12-tetraazadodecane was dissolved in 1500 ml of anhydrous dimethylform amide and then, 7.2 g (0.3 mol) of NaH was slowly added thereto in a nitrogen atmosphere. The mixture was heated for 30 minutes at a temperature of 80° C. 500 ml of dimethylform amide solution in which 129.5 g (0.16 mol) of the 3,6,9-Tris(p-tolylsulfonyl)-3,6,9-triazaundecane-1,11-dimethanesulfonate was dissolved was slowly added to the mixture at a temperature of 80° C. and then left to sit for 30 minutes. The reaction solution was cooled to room temperature, and also, cooled using iced water, and a filtered precipitate was recrystallized with acetone to produce 1,5,8,12,15,18,21-Heptakis(p-tolylsulfonyl)-1,5,8,12,15,18,21-heptaazacyclotricosane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09054392B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-784983e74d60440b809d1ad82de1a645 |
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| Source note | uspto-grants-2015_06 |
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