HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215510Generated: October 31, 2026
Pyridine → Phenyl N-(4-(1-(ethylamino)carbonyl-1H-5-indolyl)oxy-2-pyridyl)carbamate
https://huagongshe.com/reaction/2215510
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | N1-Ethyl-5-(2-amino-4-pyridyl)oxy-1H-1-indolecarboxamide | HCID 21949218 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Phenyl N-(4-(1-(ethylamino)carbonyl-1H-5-indolyl)oxy-2-pyridyl)carbamate | HCID 21949099 | 34.4% |
Reaction Steps
N1-ethyl-5-(2-amino-4-pyridyl)oxy-1H-1-indolecarboxamide (3.168 g, 10.69 mmol) synthesized in Production example 27-1 was dissolved in N,N-dimethylformamide (30 ml) under nitrogen atmosphere. Pyridine (1.25 ml, 15.40 mmol) and phenyl chlorocarbonate (1.61 ml, 12.83 mmol) were sequentially added dropwise while cooled with an ice water bath. The reaction mixture was heated to room temperature while stirred. After 1 hour, the reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the crystals were precipitated from ethyl acetate, filtered off, and dried under aeration to yield the title compound (1.530 g, 3.67 mmol, 34.4%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07109219B2 |
|---|
| Source dataset | uspto-grants-2006_09 |
|---|
| ORD ID | ord-3e509d7bed574cab91f6300a92f41094 |
|---|
| Source note | uspto-grants-2006_09 |
|---|