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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904754Generated: October 30, 2026

Potassium Carbonate → HCID 53837479, compound

https://huagongshe.com/reaction/1904754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 54085379HCID 54085379—
ReactantHCID 178527775HCID 178527775—
CatalystDimethylformamideHCID 6228—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 53837479HCID 5383747981.5%

Reaction Steps

To a mixture of 110 mg (0.483 mmol) of 3-carboxy-7-chloromethylthieno[2, 3-c]pyridine (i -5), 2 ml of dichloromethane and 2 drops of anhydrous DMF was added 0.1 ml (2.8 equivalents) of thionyl chloride, and the mixture was stirred for 2.5 hr. at room temperature. Then the solution was treated with 3 ml of anhydrous methanol, stirred for 30 min. at room temperature and refluxed for 2 min. After concentration under reduced pressure, 2 ml of anhydrous DMF, 88 mg (1.2 equivalents) of 2-mercaptobenzimidazole and 536 mg (8 quivalents) of anhydrous K2CO3 were added to the solution and the mixture was stirred for 4 hr. at room temperature. After concentration under reduced pressure, the mixture was extracted with ethyl acetate and subjected to silica gel column chromatography, eluting with CH2Cl2 --ethyl acetate. From the eluate, 140 mg (Yield : 81.5%) of 2-[(3-methoxycarbonylthieno[2, 3-c]pyridin-7-yl)methylthio]benzimidazole (Ia-10) was obtained as a foamy product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839365
Source datasetuspto-grants-1989_06
ORD IDord-cfc2f236d028416683c8e8c32387db17
Source noteuspto-grants-1989_06