HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 8-Amino-2-benzylthio-5-bromo[1,2,4]triazolo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 8-Amino-2-benzylthio[1,2,4]triazolo[1,5-a]pyridine | HCID 19080753 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Amino-2-benzylthio-5-bromo[1,2,4]triazolo[1,5-a]pyridine | HCID 21464391 | — |
Reaction Steps
8-Amino-2-benzylthio[1,2,4]triazolo[1,5-a]pyridine (25.6 g, 0.1 mol), N-bromosuccinimide (17.8 g, 0.1 mol) and 2 L of dichloromethane were combined with stirring for an hour. The solution was washed with dilute aqueous sodium bisulfite and then with water and the volatiles were removed by evaporation under reduced pressure. The residue obtained was chromatographed on silica gel eluting with 25 percent ethyl acetate in hexane. The product fractions were concentrated by evaporation under reduced pressure and the solid residue obtained was extracted with ether and dried to obtain 17.5 g (52 percent of theory) of the title compound as a light tan powder melting at 125°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700940 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-1fd487a40ce54d91a6e6baa9f9a23207 |
| Source note | uspto-grants-1997_12 |