HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromopyruvate → 2-Carbethoxy-1H-pyrrolo[1,2-c]quinazolin-4-ium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 4-Methylquinazoline | HCID 241520 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Carbethoxy-1H-pyrrolo[1,2-c]quinazolin-4-ium bromide | HCID 22756355 | — |
Reaction Steps
A solution of ethyl bromopyruvate (32.76 g, 0.172 m) and 4-methylquinazoline (15.61g, 0.109 m) in dry ethanol (400 ml) was heated at reflux for 16 hours during which time a yellow precipitate formed. The reaction mixture was cooled and the solid filtered and dried to yield crude product. Crystallization from MeOH afforded the product as a yellow solid; m.p. 274°-275° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04129653 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-15648ae6efe844828086a35b1f041296 |
| Source note | uspto-grants-1978_12 |