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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934644Generated: October 26, 2026

1-Hydroxybenzotriazole → 2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

https://huagongshe.com/reaction/1934644

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzo-1,3-dioxole-5-methylamineHCID 75799—
Reactant2-Fluoro-5-nitrobenzoic acidHCID 280997—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
Product2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamideHCID 2246764186.1%

Reaction Steps

A mixture of 2-fluoro-5-nitrobenzoic acid (1.00 g), (1,3-benzodioxol-5-ylmethyl)amine (980 mg), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (1.55 g) and 1-hydroxybenzotriazole (1.09 g) in anhydrous dimethylformamide (10 mL) was stirred for 40 hours at ambient temperature. The mixture was partitioned between water and ethyl acetate. The separated organic layer was washed with an aqueous saturated sodium bicarbonate solution, 1N-hydrochloric acid, water and brine. Then, the resultant was dried over magnesium sulfate and evaporated in vacuo. The residue was triturated with diisopropyl ether to give 2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide as yellow powders (1.48 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384080B1
Source datasetuspto-grants-2002_05
ORD IDord-829a96a6ccff41a995f08c54de850f1f
Source noteuspto-grants-2002_05