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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789781Generated: November 1, 2026

2-(difluoromethyl)-1H-1,3-benzodiazole → HCID 66669741, compound

https://huagongshe.com/reaction/1789781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(difluoromethyl)-1H-1,3-benzodiazoleHCID 597703—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 131725825HCID 131725825—
ReactantHCID 178425025HCID 178425025—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66669741HCID 6666974179%

Reaction Steps

In accordance with the procedure of the Example 4 except that 2-difluoromethylbenzimidazole in (1) of the Example 4 was replaced by 2-difluoromethyl-5-tert-butyldimethyl-silyloxybenzimidazole, obtained was 2-(2-difluoromethyl-5-tert-butyldimethylsilyloxybenzimidazol-1-yl)-4-(cis-2,3-dimethylmorpholino)-6-morpholino-1,3,5-triazine. 120 mg (0.22 mmol) of the obtained compound dissolved in THF (2 ml) was added with a solution of tetrabutylammoniumfluoride (1 M) in THF (0.5 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 75 mg (yield: 79%) of the titled compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071189B2
Source datasetuspto-grants-2006_07
ORD IDord-d9ba8b48dcf744dfb37d5d925a99469d
Source noteuspto-grants-2006_07