HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178513791, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 5-Aminoimidazole-4-carboxamide | HCID 9679 | — |
| Reactant | 4-Quinolinecarboxaldehyde | HCID 78072 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Product | HCID 178513791 | HCID 178513791 | — |
Reaction Steps
The title compound was prepared in accordance with the general method described in Example 17(e) using quinoline-4-carbaldehyde (1.0 g, 6.4 mmol), 5-aminoimidazole-4-carboxamide (0.80 g, 6.4 mmol), acetic acid (0.44 mL, 7.6 mmol) and sodium cyanoborohydride (0.48 g, 7.6 mmol) with the exception that after stirring o.n., another portion of sodium cyanoborohydride (0.48 g, 7.6 mmol) was added and the mixture heated to reflux for 4 h. After cooling to r.t., the solution was concentrated in vacuo. A portion of the 2.9 g of crude material obtained was used in the next step without further purification. MS (ESI) m/z 268 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026244B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-d3ec3dce0068405aa7b53bd75f44e39e |
| Source note | uspto-grants-2011_09 |