HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721598Generated: October 30, 2026
2-Methoxyaniline → HCID 21891184, compound
https://huagongshe.com/reaction/721598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 21890558 | HCID 21890558 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21891184 | HCID 21891184 | 80% |
Reaction Steps
2-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenoxy}acetic acid (150 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl) (122 mg), and 1-hydroxybenzotriazole hydrate (HOBT.H2O) (86 mg) were dissolved in chloroform (5 ml) to prepare a solution. o-Anisidine (63 mg) was then added to the solution, and the mixture was heated under reflux for 3 hr. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was washed with 1 N hydrochloric acid, water, and saturated brine and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin-layer chromatography using chloroform/methanol for development to give the title compound (155 mg, yield 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07135466B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-749b73019a954a96ba90b581eab13eb7 |
|---|
| Source note | uspto-grants-2006_11 |
|---|