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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710396Generated: October 29, 2026

5-(3,4-Diethoxyphenyl)-3-(1H-indol-4-yl)-1,2,4-oxadiazole → 3-(Indolin-4-yl)-5-(2-methylbenzofuran-5-yl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/710396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(3,4-Diethoxyphenyl)-3-(1H-indol-4-yl)-1,2,4-oxadiazoleHCID 25110297—
Reactant3-(1H-Indol-4-yl)-5-(2-methylbenzofuran-5-yl)-1,2,4-oxadiazoleHCID 66726607—
Product3-(Indolin-4-yl)-5-(2-methylbenzofuran-5-yl)-1,2,4-oxadiazoleHCID 66726611100%

Reaction Steps

When the product of Step D was substituted for 5-(3,4-diethoxyphenyl)-3-(1H-indol-4-yl)-1,2,4-oxadiazole in Example 34, Step C, the identical process afforded the title compound in 100% yield, as a colourless foam. 1H-NMR (CDCl3) 2.49 (s, 3H); 2.52 (broad s, 1H+H2O); 3.48 (tr, 2H, J=8.44 Hz); 3.68 (tr, 2H, J=8.44 Hz); 6.48 (s, 1H); 6.85 (d, 1H, J=7.75 Hz); 7.2 (tr, 2H, J=7.6 Hz); 7.38 (d, 1H, J=8.16 Hz); 7.51 (d, 1H, J=8.5 Hz); 8.06 (d, 1H, J=8.5 Hz); 8.32 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181182B2
Source datasetuspto-grants-2015_11
ORD IDord-2c7bc2834b614b67991b3a9e9f03907c
Source noteuspto-grants-2015_11