HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340036Generated: October 26, 2026
Benzyl Bromide → HCID 178464431, compound
https://huagongshe.com/reaction/340036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-fluoro-4-[3-(4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-6-yl]-5-(2,2,2-trifluoro-ethyl)-phenol | HCID 178516038 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178464431 | HCID 178464431 | 21.2% |
Reaction Steps
To a solution of 2-fluoro-4-[3-(4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-6-yl]-5-(2,2,2-trifluoro-ethyl)-phenol (Preparation 39, 100 mg, 168 μmol) in DMF (1 mL), was added benzyl bromide (28.8 mg, 20 μL, 168 μmol), and DIPEA (120 μL, 672 μmol). The reaction mixture was heated at 80° C. for 3 hours. The reaction mixture was then cooled to room temperature and saturated aqueous sodium hydrogen carbonate solution (5 mL) was added. The resulting solid was collected by filtration and washed with further saturated aqueous sodium hydrogen carbonate solution. The crude material was purified by HPLC Method A to afford 10.6 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895544B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-404a6798242e440aba8264bb102e8a26 |
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| Source note | uspto-grants-2014_11 |
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