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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347384Generated: October 27, 2026

Pyridine → N-[2-(5-formyl-2,4-dimethoxyphenylethynyl)phenyl]acetamide

https://huagongshe.com/reaction/347384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
Reactant5-(2-Aminophenylethynyl)-2,4-dimethoxybenzaldehydeHCID 16115620—
SolventDichloromethaneHCID 6344—
ProductN-[2-(5-formyl-2,4-dimethoxyphenylethynyl)phenyl]acetamideHCID 1143868678%

Reaction Conditions

Temperature0 °C

Reaction Steps

Pyridine (453 μL, 5.61 mmol) was added to a suspension of 5-(2-amino-phenylethynyl)-2,4-dimethoxybenzaldehyde (Ex-35C, 750 mg, 2.67 mmol) in anhydrous methylene chloride (20 mL) and chilled to 0° C. The reaction mixture was treated dropwise with acetyl chloride (9.25 mL, 75.1 mmol). Upon completion the reaction was quenched with IN HCl (10 mL) and the layers were separated. The organic layer was washed with brine, dried over sodium sulfate, and concentrated to dryness. The crude solid was purified by silica gel chromatography (5% MeOH/CH2Cl2) to yield 671 mg (78%) of N-[2-(5-formyl-2,4-dimethoxyphenylethynyl)phenyl]acetamide as an off-white solid. 1H-NMR (300 MHz, DMSO-d6) 10.15 (s, 1H), 9.23 (br s, 1H), 7.82 (m, 2H), 7.80 (s, 1H), 7.50 (dd, 1H, J=0.9, 7.8 Hz), 7.35 (dt, 1H, J=1.8, 9.3 Hz), 7.12 (t, 1H, J=7.8 Hz), 6.82 (s, 1H), 4.00 (s, 3.99 (s, 3H), 2.10 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173129B2
Source datasetuspto-grants-2007_02
ORD IDord-0e4caf59ded94fb8a9dc64cd51b6b2ef
Source noteuspto-grants-2007_02