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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364600Generated: October 31, 2026

5-Acetyl-N-(4-chloro-3-iodophenyl)thiophene-2-carboxamide → 5-acetyl-N-(4-chloro-3-(pyridin-2-yl)phenyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/1364600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Acetyl-N-(4-chloro-3-iodophenyl)thiophene-2-carboxamideHCID 66877896—
ReactantHCID 178418723HCID 178418723—
Product5-acetyl-N-(4-chloro-3-(pyridin-2-yl)phenyl)thiophene-2-carboxamideHCID 58614900—

Reaction Steps

5-Acetyl-N-(4-chloro-3-iodophenyl)thiophene-2-carboxamide (202 mg, 0.5 mmol) was used in Procedure B with 2-pyridylzincbromide (2.5 mL, 1.25 mmol, 0.5 M in THF). Purified by silica gel chromatography (10-100% ethyl acetate/hexanes) to yield 5-acetyl-N-(4-chloro-3-(pyridin-2-yl)phenyl)thiophene-2-carboxamide as a yellow solid: TLC Rf=0.19 (50% ethyl acetate/hexanes); 1H NMR (CDCl3, 400 MHz) δ 8.96 (bs, 1H), 8.67 (d, 1H), 7.79 (dt, 1H), 7.68 (m, 3H), 7.61 (d, 1H), 7.58 (d, 1H), 7.37 (d, 1H), 7.32 (m, 1H), 2.58 (s, 3H); MS (Q1) 357.0 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888364B2
Source datasetuspto-grants-2011_02
ORD IDord-f13186139ab14441b69533c5ff9b86da
Source noteuspto-grants-2011_02