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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176926Generated: November 1, 2026

Acetylacetone → 7-Fluoro-2-methyl-6-phenylamino-3H-benzoimidazole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/1176926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylacetoneHCID 31261—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 4,5-diamino-3-fluoro-2-(phenylamino)benzoateHCID 56604175—
SolventEthanolHCID 702—
Product7-Fluoro-2-methyl-6-phenylamino-3H-benzoimidazole-5-carboxylic acid methyl esterHCID 6689785791.5%

Reaction Steps

4,5-Diamino-3-fluoro-2-phenylamino-benzoic acid methyl ester 6c (0.20 g, 0.73 mmol) is suspended in ethanol (3 mL) and 5 M aqueous NCl (1 mL, 5.00 mmol) is added. The reaction mixture is brought to reflux under N2 and then 2,4-pentanedione (0.150 mL, 1.45 mmol) is added. The reaction mixture is stirred at reflux for 60 minutes. The reaction mixture is cooled to room temperature and treated with saturated aqueous NaHCO3 until the pH of the reaction mixture is pH 7 and is then concentrated under reduced pressure to dryness. The residue is diluted with ethyl acetate and water, poured into a separatory funnel and the layer separated. The ethyl layer is washed with brine, dried (Na2SO4) and concentrated under reduced pressure. The red solid residue is triturated with diethyl ether to yield a light brown solid and red filtrate. The solid is collected and washed with diethyl ether to yield 0.20 g (91%) of the pure desired product as a light brown solid. MS ESI (+) m/z 300 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842816B2
Source datasetuspto-grants-2010_11
ORD IDord-7097e5713bf349c1ac128e428a6f1b16
Source noteuspto-grants-2010_11