HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 6-(2,4-Dichloro-phenyl)-8-isobutylamino-3-morpholin-4-yl-imidazo[1,2-a]pyridine-7-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | HCID 66658969 | HCID 66658969 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-(2,4-Dichloro-phenyl)-8-isobutylamino-3-morpholin-4-yl-imidazo[1,2-a]pyridine-7-carbonitrile | HCID 66659035 | — |
Reaction Steps
In a sealed tube, a solution of 8-chloro-6-(2,4-dichloro-phenyl)-3-morpholin-4-yl-imidazo[1,2-a]pyridine-7-carbonitrile (30 mg, 0.074 mmol) and isobutylamine (0.044 mL, 0.44 mmol) in dioxane (1 mL) was heated at 110° C. for 14 h. The reaction mixture was cooled to RT, then frozen at −44° C. (dry ice) and lyophilized to give the crude 6-(2,4-dichloro-phenyl)-8-isobutylamino-3-morpholin-4-yl-imidazo[1,2-a]pyridine-7-carbonitrile intermediate. HPLC: AtRet=2.77.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097617B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-b65f22dbe2844f2387f73e489981fe91 |
| Source note | uspto-grants-2012_01 |