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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695048Generated: October 26, 2026

4-Chloro-1,2-diaminobenzene → N-(2-amino-4-chlorophenyl)-6-chloronicotinamide

https://huagongshe.com/reaction/1695048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-1,2-diaminobenzeneHCID 7263—
ReactantTriethylamineHCID 8471—
Reactant6-Chloronicotinic acidHCID 79222—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductN-(2-amino-4-chlorophenyl)-6-chloronicotinamideHCID 2266893948%

Reaction Steps

6-Chloronicotinic acid (157.5 mg, 1 mmol) and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (384 mg, 2 mmol), hydroxybenzotriazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and 4-chloro-o-phenylenediamine (171 mg, 1.2 mmol) were added. The mixture was stirred for 20 hours at room temperature. The mixture was diluted with 400 mL of brine and extracted with 200 ml of ethyl acetate. The ethyl acetate was removed under vacuum. To the residue was added 5 ml of absolute ethanol. The solids were collected by vacuum filtration, washed with absolute ethanol and dried under vacuum to give the title compound (135 mg, 48% yield) as a brown solid. LC-MS (m/z) 282 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158656B2
Source datasetuspto-grants-2012_04
ORD IDord-962de30396b64265b5287ca0bd306bc4
Source noteuspto-grants-2012_04