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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723149Generated: October 30, 2026

Potassium Carbonate → HCID 69586224, compound

https://huagongshe.com/reaction/723149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Bromomethyl)-1,3-difluorobenzeneHCID 581435—
ReactantHCID 178498675HCID 178498675—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductAmmoniaHCID 222—
ProductHCID 69586224HCID 69586224115.9%
ProductHCID 69586394HCID 69586394—

Reaction Steps

A solution of 4-(7-chloro-1H-benzoimidazole-5-sulfonyl)-5-methylsulfanyl-thiophene-2-carboxylic acid methyl ester ((from above step c) 0.201 g, 0.499 mmol) in DMF (4 mL) was treated with α-bromo-2,6-difluorotoluene (0.114 g, 0.549 mmol) and solid K2CO3 (0.152 g, 1.10 mmol). The reaction was stirred at room temperature 17 h, diluted with EtOAc and washed well with water (5×150 mL). The organic layer was dried over MgSO4 and concentrated in vacuo. Silica gel chromatography (2% MeOH with 2 M NH3 in CH2Cl2) afforded the products 4-[7-chloro-3-(2,6-difluoro-benzyl)-3H-benzoimidazole-5-sulfonyl]-5-methylsulfanyl-thiophene-2-carboxylic acid methyl ester and 4-[7-chloro-1-(2,6-difluoro-benzyl)-1H-benzoimidazole-5-sulfonyl]-5-methylsulfanyl-thiophene-2-carboxylic acid methyl ester (0.102 g, 38%). These isomers were not separable by silica gel chromatography, but they were carried on together into the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138530B2
Source datasetuspto-grants-2006_11
ORD IDord-70af8efd1d0f4fd8b580ddd96fbd25ac
Source noteuspto-grants-2006_11