HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium → 3-(2-Fluorobenzyl)imidazo[1,5-a]pyridine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium | HCID 223 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ethyl 3-(2-fluorobenzyl)imidazo[1,5-a]pyridine-1-carboxylate | HCID 59177857 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Fluorobenzyl)imidazo[1,5-a]pyridine-1-carboxamide | HCID 59177870 | — |
Reaction Steps
560 mg (1.88 mmol) of ethyl 3-(2-fluorobenzyl)imidazo[1,5-a]pyridine-1-carboxylate from example 7A are heated in 55 ml of 33% strength aqueous ammonium solution in a microwave at 130° C. for 3 h. The mixture is diluted with water, and, after addition of some methanol, extracted with ethyl acetate. The organic phase is dried over sodium sulfate and concentrated. 229 mg (87.5% purity, 40% of theory) of the desired compound are obtained as greenish crystals which are reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309551B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-86fef6edfb0f44dcb6b9b9e3cb2bffa9 |
| Source note | uspto-grants-2012_11 |