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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010066Generated: November 1, 2026

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

https://huagongshe.com/reaction/1010066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
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 HCl (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 layers separated. The ethyl acetate 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 a 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 numberUS07973170B2
Source datasetuspto-grants-2011_07
ORD IDord-d82402d4cb6943ab8a5fc276e8a2adfa
Source noteuspto-grants-2011_07