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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174945Generated: October 31, 2026

Pyridine → HCID 57771747, compound

https://huagongshe.com/reaction/1174945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(4-Fluorophenyl)benzoic acidHCID 2782689—
ReactantHCID 57771701HCID 57771701—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 57771747HCID 5777174744%

Reaction Steps

Add oxalyl chloride (0.20 mL, 2.30 mmol) and 4 drops of DMF to a stirring suspension of 4′-fluoro-biphenyl-4-carboxylic acid (0.243 g, 1.13 mmol) in CH2Cl2 (5.0 mL). Stir the reaction mixture at room temperature for 2 h. Concentrate the mixture in vacuo, add n-hexane, re-concentrate, and re-dissolve in CH2Cl2. Add the resultant 4′-fluoro-biphenyl-4-carbonyl chloride solution to a mixture of rac-N-{2-[(6-amino-benzothiazol-2-yl)-methyl-amino]-ethyl}-N-methyl-acetamide (0.146 g, 0.524 mmol) and pyridine (0.06 mL) in CH2Cl2 (10 mL). Shake the reaction mixture overnight at room temperature. Subject the residue to silica gel flash column chromatography (3×4 g columns, eluting with 5-10% ethyl acetate/n-hexane to remove impurities, then flushing off product with 2N NH3/MeOH). Triturate the residue with CH2Cl2 to yield the desired product as a white solid (0.110 g, 44%). mass spectrum (m/e): 477.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838543B2
Source datasetuspto-grants-2010_11
ORD IDord-050da7f8803f4e1da0cb208c1404a38e
Source noteuspto-grants-2010_11