Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 68089304 | HCID 68089304 | — |
| Product | HCID 68089376 | HCID 68089376 | — |
Reaction Steps
To 2-{1-[(1-{[(R)-5-(4-cyano-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carbonyl]-amino}-cyclopropanecarbonyl)-amino]-cyclopropyl}-isonicotinic acid (30 mg, 0.044 mmol), in DMF (3 mL) was added HATU (50 mg, 0.13 mmol) diisopropylethylamine (23 μL, 0.13 mmol) and mono-Boc-protected ethylenediamine (14 mg, 0.088 mmol). The reaction was shaken at room temperature overnight. Water was added (0.1 mL) and the crude reaction was purified by HPLC to afford {2-[(6-{1-[(1-{[(R)-5-(4-cyano-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carbonyl]-amino}-cyclopropanecarbonyl)-amino]-cyclopropyl}-pyridine-3-carbonyl)-amino]-ethyl}-carbamic acid tert-butyl ester. This material was dissolved in dichloromethane (1.0 mL) and 4M HCl in dioxane (0.5 mL) was added. The reaction was shaken for 2 h at room temperature. The volatiles were removed to afford 23 mg of the title compound, m/z 726.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481750B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-9d4460f77cac446ab9fc3f000f247f67 |
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| Source note | uspto-grants-2013_07 |
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