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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389433Generated: October 26, 2026

4-Iodo-2-(isoquinolin-5-yl)furo[2,3-c]pyridin-7-amine → 2-(1-Benzothiophen-7-yl)-4-iodofuro[2,3-c]pyridin-7-amine

https://huagongshe.com/reaction/389433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-2-(isoquinolin-5-yl)furo[2,3-c]pyridin-7-amineHCID 66759474—
Reactant2-(1-Benzothiophen-7-yl)furo[2,3-c]pyridin-7-amineHCID 66760270—
Product2-(1-Benzothiophen-7-yl)-4-iodofuro[2,3-c]pyridin-7-amineHCID 6675997551%

Reaction Steps

The title compound was prepared in 51% yield from 2-(1-benzothiophen-7-yl)furo[2,3-c]pyridin-7-amine by a procedure analogous to Intermediate 10, Step B. 1H NMR (300 MHz, DMSO-d6) δ 8.20 (d, J=7.5 Hz, 1H), 8.01 (d, J=7.6 Hz, 1H), 7.95 (d, J=1.5 Hz, 2H), 7.64-7.58 (m, 2H). 7.18 (s, 1H). 6.67 (br s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-c126ca1747fb473e86aa382492d6784f
Source noteuspto-grants-2013_02