HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → HCID 13089302, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | HCID 4164963 | HCID 4164963 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 13089302 | HCID 13089302 | 67% |
Reaction Steps
Into 45 ml of o-xylene, were added 1.5 g of ethyl N-(4-phenyl-2-thiazolyl)carbamate and 4.0 g of 2-aminopyridine. The mixture was stirred for 2.5 hours under refluxing. The reaction solution was allowed to stand for cooling. Deposited crystals were collected by filtration and washed with methyl alcohol. The crystals were then recrystallized from an N,N-dimethylformamide/methyl alcohol mixed solvent to obtain 1.2 g of N-(2-pyridyl)-N'-(4-phenylthiazol-2-yl)urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04490393 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-e8e18761dcc44cb6aa48ac5c6e401c79 |
| Source note | uspto-grants-1984_12 |