HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-ethyl-4-chloro-7-carboxy-1H-pyrazolo[3,4-b]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-(1-ethylpyrazol-5-yl)-4-carboxyanthranilic acid | HCID 21217714 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-ethyl-4-chloro-7-carboxy-1H-pyrazolo[3,4-b]quinoline | HCID 21217704 | — |
Reaction Steps
A mixture of N-(1-ethylpyrazol-5-yl)-4-carboxyanthranilic acid (2.5 g) and POCl3 (20 ml) is refluxed overnight. The reaction mixture is poured into water, acidified with acetic acid, and the solids which form are collected by filtration. The solid is taken up in 10% NaOH, washed with ether and then the aqueous layer is acidified with concentrated HCl. The mixture is extracted with ether, the ether layer is dried over MgSO4 filtered and evaporated to afford 1 g of 1-ethyl-4-chloro-7-carboxy-1H-pyrazolo[3,4-b]quinoline, as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05942520 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-a5e3ed1e265449028f28dc3804e27863 |
| Source note | uspto-grants-1999_08 |