HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → 5-(p-Tert-butylaminocarbonylphenyl)imidazo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(p-Carboxyphenyl)imidazo[1,5-a]pyridine | HCID 13688224 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(p-Tert-butylaminocarbonylphenyl)imidazo[1,5-a]pyridine | HCID 13688225 | — |
Reaction Steps
To a slurry of 0.4 g of 5-(p-carboxyphenyl)imidazo[1,5-a]pyridine in 40 ml of methylene chloride under nitrogen at room temperature, is added 30 μl of N,N-dimethylformamide followed by 0.16 ml of oxalyl chloride. The reaction mixture is stirred until gas evolution is complete and 0.46 ml of tert-butylamine is added dropwise. Stirring is discontinued after 90 min and 10 ml of saturated sodium bicarbonate solution is added. The organic layer is separated, dried over sodium sulfate and evaporated to yield the title compound, m.p. 128°-131°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428160 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-bceb03b365eb4b88a809530aadc48735 |
| Source note | uspto-grants-1995_06 |