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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524425Generated: November 4, 2026

3-Cyanophenylboronic acid → HCID 71259691, compound

https://huagongshe.com/reaction/1524425

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyanophenylboronic acidHCID 2734325—
Reactant3-Bromo-N-(2,4-Dimethoxybenzyl)-1-Methyl-N-(1,2,4-Thiadiazol-5-yl)-1H-Indole-6-SulfonamideHCID 71259222—
ProductHCID 71259691HCID 71259691—

Reaction Steps

The title compound was prepared in an analogous manner to that described in Example 28 using (3-cyanophenyl)boronic acid and 3-bromo-N-(2,4-dimethoxybenzyl)-1-methyl-N-(1,2,4-thiadiazol-5-yl)-1H-indole-6-sulfonamide, and the desired product, 3-(3-cyanophenyl)-1-methyl-N-(1,2,4-thiadiazol-5-yl)-1H-indole-6-sulfonamide, was isolated as an off-white solid. 1H NMR (500 MHz, DMSO-d6) δ ppm 3.90 (s, 3 H) 7.56 (dd, J=8.48, 1.60 Hz, 1 H) 7.61-7.69 (m, 2 H) 7.86-7.92 (m, 2 H) 7.94-8.07 (m, 4 H). m/z (ESI) 395.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079902B2
Source datasetuspto-grants-2015_07
ORD IDord-b585d6b7553b49979b9eecfd30a0f4d4
Source noteuspto-grants-2015_07