HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 6-iodoimidazo[1,2-a]pyridine-2-carboxylate → 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 6-iodoimidazo[1,2-a]pyridine-2-carboxylate | HCID 3681971 | — |
| Reactant | 6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide | HCID 24771673 | — |
| Product | 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide | HCID 44135939 | — |
Reaction Steps
By working in the same manner as for the preparation of Intermediate 1, replacing the ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate with ethyl 6-iodoimidazo[1,2-a]pyridine-2-carboxylate, 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide is obtained in the form of a beige-coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314109B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-80fac43816284c88a464200adbd18c09 |
| Source note | uspto-grants-2012_11 |