HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 86596411, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(Quinolin-6-yl)-1H-indole-3-carboxylic acid | HCID 68968514 | — |
| Product | HCID 86596411 | HCID 86596411 | — |
Reaction Steps
20 cm3 of thionyl chloride are added at 22° C. under an argon atmosphere to 0.69 g (2.1 mmol) of 3-carboxy-1-(quinol-6-yl)-1H-indole. After stirring at reflux for 4 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa). The residue is successively triturated twice with 10 cm3 of dimethoxyethane and then concentrated to dryness under reduced pressure (2.7 kPa) to give 1 g of 3-chlorocarbonyl-1-(quinol-6-yl)-1H-indole hydrochloride in the form of an orange-coloured solid which is used directly in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531663B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-58353114c3a446408dac349b47561391 |
| Source note | uspto-grants-2009_05 |