Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 67194147 | HCID 67194147 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 52934784 | HCID 52934784 | 39.6% |
Reaction Steps
Concentrated HCl (3 mL) was added to a stirred solution of 7-(4-bromo-2-fluoro-phenylamino)-8-[1-(2,3-dihydroxy-propyl)-cyclopropanesulfonylamino]-6-methyl-5-oxo-2,3-dihydro-5H-imidazo[1,2-a]pyridine-1-carboxylic acid tert-butyl ester (75 mg) in THF (10 mL). The resulting mixture was stirred at 45° C. for 1 hour. The reaction was monitored by TLC (10% MeOH in CHCl3). The reaction mixture was concentrated and partitioned between ethyl acetate and water. The organic layer was washed with saturated NaHCO3 solution and concentrated to afford 25 mg of the product (39.58% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08466289B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-dba8b08320424506b87d16b631e03698 |
|---|
| Source note | uspto-grants-2013_06 |
|---|