HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 19913604, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | HCID 15027560 | HCID 15027560 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19913604 | HCID 19913604 | 33% |
Reaction Steps
A mixture of 7-propyl-3,4-dihydro-2H,5H-pyrimido[6,1-b][1,3]thiazine-6,8(7H)-dione (1 g), paraformaldehyde (0.22 g) and dimethylamine hydrochloride (0.51 g) in acetic acid (25 ml) was refluxed for 18 hours. The reaction solution was concentrated dryness, and the resulting residue was dissolved in water. Then, the solution was made basic with 1N aquaous sodium hydroxide, followed by extraction of the product with methylene chloride. After washing with water and drying, the organic layer was concentrated to dryness to obtain a syrup. The syrup was converted to the hydrochloride to form crystals, which were recrystallized from ethanol-ethyl acetate to give colorless prisms (0.46 g, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05082838 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-1f64d4a8bcfd45d39bb9bffcf86d2422 |
| Source note | uspto-grants-1992_01 |