HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-(Indol-3-yl)-4-carboxy-6,7-dimethoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(N-phenylsulfonylindol-3-yl)-4-carboxy-6,7-dimethoxyquinoline | HCID 18788613 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Indol-3-yl)-4-carboxy-6,7-dimethoxyquinoline | HCID 18788709 | — |
Reaction Steps
A stirred solution of (0.547 g) of 2-(N-phenylsulfonylindol-3-yl)-4-carboxy-6,7-dimethoxyquinoline, K2CO3 (0.380 g), MeOH (40 ml) and H2O (10 ml) are heated to reflux. The MeOH is evaporated in vacuo, and the aqueous residue diluted with more H2O, and acidified with 0.IN HCl to pH between 6°-7 while contained in an ice-bath. An orange solid precipitates. This is collected, washed with ether then dried under vacuum (0.1 mm at 22° C.) for a few hours to obtain 2-(indol-3-yl)-4-carboxy-6,7-dimethoxyquinoline m.p. 286° C. dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05480883 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-acebd435d0cd43bbba845b188e5dc070 |
| Source note | uspto-grants-1996_01 |