HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloroquinazoline → Ethyl 1-quinazolin-4-ylindolin-3-ylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloroquinazoline | HCID 78864 | — |
| Reactant | Ethyl (2,3-dihydro-1H-indol-3-yl)acetate | HCID 21795444 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 1-quinazolin-4-ylindolin-3-ylacetate | HCID 54457736 | — |
Reaction Steps
A mixture of 4-chloroquinazoline (2.3g.) and ethyl indolin-3-ylacetate (2.6g.) in 1,2-dimethoxyethane (30ml.) was heated under reflux for 15 minutes. The mixture was cooled and filtered, and the solid residue was dissolved in ice-water (40ml.). To the solution was added saturated sodium acetate solution (10ml.), and the mixture was extracted with ethyl acetate (3 × 50ml.). The combined extracts were dried (Na2SO4), and the solvent evaporated in vacuo to give ethyl 1-quinazolin-4-ylindolin-3-ylacetate as a syrup which was proved to be pure by TLC (system A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04012513 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-dcde0069e29d44d29c10c2b03b9f218d |
| Source note | uspto-grants-1977_03 |