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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716419Generated: November 2, 2026

Chloroacetonitrile → HCID 16059409, compound

https://huagongshe.com/reaction/1716419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantSodium hydrideHCID 24758—
ReactantHCID 16059348HCID 16059348—
SolventDimethylformamideHCID 6228—
ProductHCID 16059409HCID 1605940914%

Reaction Steps

To a stirred solution of 40 mg (0.101 mmol) of 1-[1-(6-Chloro-1H-indole-3-carbonyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one (the preparation of which has been described in example 18) in 5 ml DMF was added 4.2 mg (0.105 mmol) NaH (60% in oil). The mixture was stirred at RT for 30 min. and then 8.3 mg (0.11 mmol) of chloro-acetonitrile was added. The mixture was stirred an additional hour and then poured onto water and extracted with ethyl acetate. The combined organic phases were dried over Na2SO4 and concentrated in vacuo. Preparative HPLC afforded 6 mg (14%) of {6-Chloro-3-[4-(2-oxo-2,3-dihydro-benzoimidazol-1-yl)-piperidine-1-carbonyl]-indol-1-yl}-acetonitrile as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803815B2
Source datasetuspto-grants-2010_09
ORD IDord-3fe02dac9e4b4e96b6d83f1764b5e407
Source noteuspto-grants-2010_09