Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040238Generated: October 31, 2026

Diisopropylethylamine → N-(3-(1,3,4-oxadiazol-2-yl)phenyl)-4-bromopicolinamide

https://huagongshe.com/reaction/1040238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromopyridine-2-carboxylic acidHCID 735150—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-(1,3,4-Oxadiazol-2-yl)anilineHCID 16228097—
SolventDimethylformamideHCID 6228—
ProductN-(3-(1,3,4-oxadiazol-2-yl)phenyl)-4-bromopicolinamideHCID 5810293281%

Reaction Steps

A solution of 4-bromopyridine-2-carboxylic acid (3.76 g, 18.6 mmol), 3-[1,3,4]oxadiazol-2-yl-phenylamine (3.0 g, 18.6 mmol), (2-(7-Aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU) (7.1 g, 18.7 mmol), and diisopropylethylamine (15 mL) in N,N-dimethylformamide was stirred at room temperature for 1 hour. The solvent was removed under reduced pressure, and the residue was stirred with acetonitrile (40 mL) and water (40 mL). The solid thus obtained was isolated by filtration, washed with water (20 mL), acetonitrile (20 mL) and diethyl ether (40 mL), and dried under reduced pressure to give N-(3-(1,3,4-oxadiazol-2-yl)phenyl)-4-bromopicolinamide as a white powder (5.2 g, 15.0 mmol, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552196B2
Source datasetuspto-grants-2013_10
ORD IDord-e3c7293359f2408e9452081753580b29
Source noteuspto-grants-2013_10