Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diphenylphosphoryl azide | HCID 123414 | — |
| Reactant | HCID 57961678 | HCID 57961678 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57962653 | HCID 57962653 | 55% |
Reaction Steps
To a solution of 6-chloro-2,4,8,22-tetraazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene-11-carboxylic acid (9.2 mg, 25.1 μmol) in tert-butyl alcohol (0.16 mL) was added triethylamine (3.5 μL, 25.1 μmol) and diphenylphosphonic azide (5.4 μL, 25.1 μmol). The resulting mixture was heated at 85° C. overnight. The reaction mixture was diluted with DMSO and purified with preparative LCMS to give the desired product (6 mg, 55%). 1H NMR (400 MHz, DMSO-d6): δ 9.33 (s, 1H), 9.22 (s, 1H), 8.09 (s, 1H), 7.92 (s, 1H), 7.31 (m, 2H), 7.08 (t, 1H), 7.03 (s, 1H), 6.88 (dd, 1H), 6.80 (dd, 1H), 2.80 (d, 4H), 1.46 (s, 9H). LCMS calculated for C23H25ClN5O2(M+H)+: m/z=438.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871753B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-069317e56b5741c08300fe54a2d3dbb5 |
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| Source note | uspto-grants-2014_10 |
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