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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946245Generated: November 2, 2026

Oxalyl chloride → HCID 178491050, compound

https://huagongshe.com/reaction/1946245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Cyano-2-methoxybenzoyl chlorideHCID 21275322—
Reactant5-Cyano-2-methoxybenzoic acidHCID 21942568—
ReactantHCID 178508054HCID 178508054—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178491050HCID 17849105011.9%

Reaction Steps

5-Cyano-2-methoxy-benzoic acid (Example 1F) (40 mg, 0.22 mmol) was dissolved in DCM (5 ml) and oxalyl chloride (34.4 mg, 0.264 mmol) was then added drop wise followed by DMF (1 drop). The reaction mixture was stirred at ambient temperature for 1 hour, reduced in vacuo, then re-evaporated using toluene (×2). A mixture of 3-(5-morpholin-4-ylmethyl-1H-benzimidazol-2-yl)-1H-pyrazol-4-ylamine (100 mg, 0.33 mmol), 5-cyano-2-methoxy-benzoyl chloride and diisopropylethylamine (1.83 μl, 0.9 mmol) in THF (5 ml) was stirred at 0° C. and then allowed to warm to room temperature over 2 hours. The reaction mixture was then concentrated in vacuo. The residue was purified by flash column chromatography SiO2, 5-7% MeOH-DCM] to give 5-cyano-2-methoxy-N-[3-(5-morpholin-4-ylmethyl-1H-benzoimidazol-2-yl)-1H-pyrazol-4-yl]-benzamide (12 mg). (LC/MS Acidic: Rt 2.02 min [M−H]+458).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399442B2
Source datasetuspto-grants-2013_03
ORD IDord-85a248a922774a20bb47ae4240c2ed0b
Source noteuspto-grants-2013_03