HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → 6-Bromo-N-(2-thiazolyl)pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | (6-Bromo-pyridin-2-YL)thiourea | HCID 22170428 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Bromo-N-(2-thiazolyl)pyridin-2-amine | HCID 22170401 | 96% |
Reaction Steps
A suspension of 2-bromo-6-thioureidopyridine (3 g, 12.92 mmol) and chloroacetaldehyde (3.28 mL, 25.85 mmol) in ethanol (27 mL) and water (7 mL) was heated at reflux for 4.75 h. The solution was concentrated in vacuo and the residue was diluted with 1 N aqueous NaOH solution at 0° C., stirred for 10 min, and the pH was then adjusted to 8.5 by addition of 6 N aqueous HCl solution. The precipitate was collected by filtration, washed several times with water and dried in vacuo over P2O5 to obtain the titled compound (3.17 g, 96%) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706717B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-6008bb2fbb9e4cdab9922f9daf64bc80 |
| Source note | uspto-grants-2004_03 |