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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904747Generated: November 1, 2026

Dimethylformamide → HCID 14461486, compound

https://huagongshe.com/reaction/1904747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14461480HCID 14461480—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 14461486HCID 14461486—

Reaction Steps

To 44.0 mg (1.10 mmol) of 60% NaH were added 7 ml of dry DMF and 299.2 mg (1.00 mmol) of 2-[(thieno[2, 3-c]pyridin-7-yl)methylthio]benzimidazole. 1/10 H2O (Ia-1). After stirring for 10 min. at room temperature, the solution was added with 130.2 mg (1.20 mmol) of ClCOOEt and stirred for 30 minutes at room temperature. DMF was evaporated under reduced pressure. Water was added to the residue, and the solution was extracted with CH2Cl2. After drying over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, whereby 381.0 mg of pale greenish yellow cyrstals were obtained. After being subjected to silica gel column chromatography, the crystals were dispersed with 2 ml of ether, followed by filtration and washed with ether, whereby 335.7 mg (Yield : 90.9%) of the objective compound, 1-ethoxycarbonyl-2-[(thieno[2, 3-c]pyridin-7-yl)methylthio]benzimidazole (Ib-1) was obtained as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839365
Source datasetuspto-grants-1989_06
ORD IDord-c2a828411bd84355bc65f5327ec67ddf
Source noteuspto-grants-1989_06