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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789782Generated: November 1, 2026

2-(difluoromethyl)-1H-1,3-benzodiazole → HCID 22036898, compound

https://huagongshe.com/reaction/1789782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(difluoromethyl)-1H-1,3-benzodiazoleHCID 597703—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 22036893HCID 22036893—
ReactantHCID 57420451HCID 57420451—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22036898HCID 2203689893%

Reaction Steps

In accordance with the procedure of the Example 1 except that 2-difluoromethylbenzimidazole in (1) of the Example 1 was replaced by 2-difluoromethyl-5-tert-butyldimethylsilyloxybenzimidazole, obtained was 2-(2-difluoromethyl-5-tert-butyldimethylsilyloxybenzimidazol-1-yl)-4,6-dimorpholinopyrimidine. 0.55 g (1.0 mmol) of the obtained compound dissolved in THF (10 ml) was added with a solution of tetrabutylammoniumfluoride (1 M) in THF (2 ml) and stirred at room temperature for 30 minutes. The reaction solution was poured into water and extracted with ethyl acetate. The separated organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography to obtain 0.40 g (yield: 93%) of the titled compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071189B2
Source datasetuspto-grants-2006_07
ORD IDord-1e6a466c51cc492e9ad3e90bd07420f0
Source noteuspto-grants-2006_07