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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247123Generated: October 25, 2026

3-Nitrobenzaldehyde → HCID 135833417, compound

https://huagongshe.com/reaction/247123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
Reactant5-Acetonyl-3-chloromethyl-1,2,4-oxadiazoleHCID 13824705—
Reactant5-(2-Amino-1-propenyl)-3-chloromethyl-1,2,4-thiadiazoleHCID 70054050—
SolventIsopropanolHCID 3776—
ProductHCID 135833417HCID 13583341715.5%

Reaction Steps

A stirred mixture of 343 mg of 5-(2-amino-1-propenyl)-3-chloromethyl-1,2,4-thiadiazole, 316 mg of 5-acetonyl-3-chloromethyl-1,2,4-oxadiazole and 273 mg of 3-nitrobenzaldehyde in 5 ml of isopropyl alcohol was heated under reflux for 10 hours. The mixture was concentrated in vacuo and the residue was chromatographed on silica gel using benzene-ethyl acetate (5:1) as eluent to give 134 mg of 1,4-dihydro-2,6-dimethyl-3-(3-chloromethyl-1,2,4-oxadiazol-5-yl)-5-(3-chloromethyl-1,2,4-thiadiazol-5-yl)-4-(3-nitrophenyl)pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04705786
Source datasetuspto-grants-1987_11
ORD IDord-d2e17b014b244f50b927dd81982f8200
Source noteuspto-grants-1987_11