HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 58574749, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 6,8,9,10,11,13-Hexahydro-13-oxo-7H-azocino[2,1-b]quinazoline-3-carboxylic acid | HCID 7130615 | — |
| Reactant | HCID 178418247 | HCID 178418247 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 58574749 | HCID 58574749 | — |
Reaction Steps
A solution of 13-oxo-7,8,9,10,11,13-hexahydro-6H-azocino[2,1-b]quinazoline-3-carboxylic acid (100 mg, 0.37 mmol), acetaldehyde (5 mL) and CH3COONa (1 g) in acetic acid (10 mL) was stirred at 110° C. for 24 hours. After it was cooled to room temperature, the mixture was adjusted to pH around 8 with Na2CO3 and extracted with a mixture of dichloromethane/methanol (10/1) (3×30 mL). The combined organic layers were washed with brine and dried over Na2SO4. After filtration and concentration, the crude product obtained was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772301B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-06730f6f82374f7894042bb3024f42c0 |
| Source note | uspto-grants-2014_07 |