HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2-butanone → N-(2-Ethylimidazo[1,2-a]pyrid-6-yl)-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2-butanone | HCID 13156 | — |
| Reactant | N-[6-aminopyrid-3-yl]-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamide | HCID 66863527 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2-Ethylimidazo[1,2-a]pyrid-6-yl)-5-fluoro-1-[(3-fluorophenyl)methyl]-1H-indole-2-carboxamide | HCID 66864699 | 100.1% |
Reaction Steps
Compound 5 was prepared according to a process similar to that described in step 4.3, by reacting 0.1 g (0.26 mmol) of N-[6-aminopyrid-3-yl]-5-fluoro-1-[(3-fluorophenyl)-methyl]-1H-indole-2-carboxamide, prepared according to the protocol described in step 4.2, with 0.08 g (0.53 mmol) of 1-bromobutan-2-one in 4 mL of acetonitrile. 0.112 g of the expected product is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394820B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-c662ed0baf534f1fade9d8bd81b375fd |
| Source note | uspto-grants-2013_03 |