Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898815Generated: November 3, 2026

N-bromobutanimide → 8-Amino-2-benzylthio-5-bromo[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1898815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant8-Amino-2-benzylthio[1,2,4]triazolo[1,5-a]pyridineHCID 19080753—
SolventDichloromethaneHCID 6344—
Product8-Amino-2-benzylthio-5-bromo[1,2,4]triazolo[1,5-a]pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571775
Source datasetuspto-grants-1996_11
ORD IDord-7a5f43305bd94912b247faa6037771f2
Source noteuspto-grants-1996_11