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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(difluoromethyl)-1H-1,3-benzodiazole | HCID 597703 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 131725825 | HCID 131725825 | — |
| Reactant | HCID 178425025 | HCID 178425025 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66669741 | HCID 66669741 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071189B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-d9ba8b48dcf744dfb37d5d925a99469d |
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| Source note | uspto-grants-2006_07 |
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