Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 178513230 | HCID 178513230 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178473664 | HCID 178473664 | 45% |
Reaction Steps
2-(4-Fluoro-phenyl)-N-hydroxy-imidazo[1,2-a]pyridine-6-carboxamidine (example 56; 85.1 mg, 0.315 mmol) was dissolved in 5 ml DMF. The mixture was heated to 80° C. after addition of triethylamine (87.8 μl, 0.63 mmol) and ethyl chloroformate (33 μl, 0.34 mmol) for 2.5 hours. The mixture was evaporated. Ethyl acetate and water were added, the organic layer was separated, washed with water, dried and evaporated. The crude product was purified by preparative HPLC (RP18, acetonitrile/water 0.1% TFA) to yield 48 mg (45%) of the desired product. MS: M+H+=343.05.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08399476B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d972b9a90f0849a8adc9f7364a96ceaf |
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| Source note | uspto-grants-2013_03 |
|---|