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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593572Generated: October 25, 2026

4-Amino-3-iodobenzonitrile → 2-(4-methoxy-pyridin-3-yl)-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/593572

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3-iodobenzonitrileHCID 4416395—
Reactant3-Ethynyl-4-methoxypyridineHCID 58215706—
Product2-(4-methoxy-pyridin-3-yl)-1H-indole-5-carbonitrileHCID 58215634—

Reaction Steps

4-Methoxy-3-ethynyl-pyridine and 4-cyano-6-iodoaniline are processed according to the method described in Example 86 to give 2-(4-methoxy-pyridin-3-yl)-1H-indole-5-carbonitrile. 2-(4-Methoxy-pyridin-3-yl)-1H-indole-5-carbonitrile is purified by HPLC using an Xbridge Shield RP18 with a gradient of acetonitrile in 0.1% NH4OH. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.04 (s, 3H), 7.14 (d, J=1.3 Hz, 1H), 7.25 (d, J=5.8 Hz, 1H), 7.47 (dd, J=8.5, 1.6 Hz, 1H), 7.61 (d, J=8.3 Hz, 1H), 8.11 (s, 1H), 8.47 (d, J=5.8 Hz, 1H), 8.91 (s, 1H), 11.91 (br. s., 1H). HRMS (ESI) m/z 250.0968 [(M+H)+ calcd for C15H12N3O: 250.0980].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242963B2
Source datasetuspto-grants-2016_01
ORD IDord-dc9de4c4ce5b4d029179ce744c58defe
Source noteuspto-grants-2016_01