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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041752Generated: October 25, 2026

Triethylamine → N-ethyl-5-(2-nitrophenyl)-1,3,4-oxadiazol-2-amine

https://huagongshe.com/reaction/1041752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Ethyl-1-(2-nitrobenzoyl)semicarbazideHCID 47252607—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-ethyl-5-(2-nitrophenyl)-1,3,4-oxadiazol-2-amineHCID 6726462061.9%

Reaction Steps

A mixture of 4-ethyl-1-(2-nitrobenzoyl)semicarbazide (4 g) in DCM (30 mL) was treated with triethyl amine (12 mL), PTS-Cl (4.8 g) and DMAP (100 mg). The reaction mixture was stirred for 4 hours, concentrated, and purified by silica gel chromatography to afford 2.3 g of ethyl-(5-(2-nitro-phenyl)-(1,3,4)oxadiazol-2-yl)-amine: 1H NMR (300 MHz, CDCl3) δ 8.1 (dd, 1H), 8.0 (d, 1H), 7.8 (m, 2H), 4.9 (bs, 1H), 3.6 (q, 2H), 1.4 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-e80e3622416f47e7ae0da8216412e1cc
Source noteuspto-grants-2013_10