HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 7-Bromo[1,2,4]triazolo[1,5-a]pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 57643101 | HCID 57643101 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Bromo[1,2,4]triazolo[1,5-a]pyridin-2-amine | HCID 54594025 | 87.4% |
Reaction Steps
A mixture of hydroxylamine hydrochloride (20.0 g, 288 mmol) and N-ethyldiisopropylamine (30.1 ml, 173 mmol) in ethanol (367 ml) is stirred for a few minutes at room temperature and the mixture is added to 1-ethoxycarbonyl-3-(4-bromo-pyridin-2-yl)-thiourea (17.5 g, 57.5 mmol). The resulting mixture is refluxed for 1 day. The solvent is evaporated and 100 ml water is added to the residue. The suspension is stirred for 10 minutes, the solid is collected by filtration, washed with water and dried affording 7-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine (10.71 g, 87.4%) as a light yellow solid. Mp.: 190-2° C. MS: m/z=213.0, 215.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349824B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-afa48e4c5ab44df6a07a1212b8426b53 |
| Source note | uspto-grants-2013_01 |