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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157455Generated: October 27, 2026

Oxalyl chloride → HCID 44203076, compound

https://huagongshe.com/reaction/1157455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-N-isopropylacetamideHCID 533849—
Reactant5-Fluoro-2-nitrobenzoic acidHCID 2737420—
SolventDichloromethaneHCID 6344—
ProductHCID 44203076HCID 44203076365.4%

Reaction Steps

To a solution of 5-fluoro-2-nitrobenzoic acid (2.3 g, 12.4 mmol) in dichloromethane (20 mL) was added oxalyl chloride (3.2 g, 2.2 mL, 24.8 mmol) dropwise. After 1 h the solution was concentrated to dryness. 2-Amino-N-isopropylacetamide (INTERMEDIATE I.1) (0.30 g, 2.6 mmol) was dissolved in dichloromethane (20 mL) and diisopropylethylamine (DIEA) (6.8 mL, 38.9 mmol) added. The acid chloride in dichloromethane (10 mL) was added dropwise and the reaction mixture stirred at room temperature for 18 h. The reaction mixture was concentrated in vacuo, the residue dissolved in dichloromethane and washed with 1 N NaOH (aq.), 1 N HCl (aq.) and brine. The organic layers were dried (MgSO4) and concentrated in vacuo to yield 5-fluoro-N-(isopropylcarbamoylmethyl)-2-nitrobenzamide (2.7 g, 9.5 mmol, 81%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807686B2
Source datasetuspto-grants-2010_10
ORD IDord-37d8fff495794000bc6c90810a8e2a40
Source noteuspto-grants-2010_10