HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594955Generated: October 30, 2026
alpha-Bromo-o-fluorotoluene → HCID 56942350, compound
https://huagongshe.com/reaction/594955
Participants
| Role | Name | HCID | Charge |
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| Reactant | alpha-Bromo-o-fluorotoluene | HCID 67968 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 66807042 | HCID 66807042 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 56942350 | HCID 56942350 | — |
Reaction Steps
Dichloromethane (1.78 mL) was added to N-((1S,5R)-8-azabicyclo[3.2.1]octan-2-yl)-3-(1-methyl-1H-indazol-5-yl)-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxamide (72.3 mg, 0.178 mmol) in a flask. 2-Fluorobenzylbromide (0.0214 mL, 0.178 mmol) was added to the reaction. At room temperature, diisopropylethylamine (0.0920 mL, 0.534 mmol) was added dropwise to the reaction. The reaction was allowed to stir at room temperature for 1 hr. The reaction was quenched using water, was extracted three times using dichloromethane. The dichloromethane extractions were combined, dried over sodium sulfate, filtered, and concentrated. The crude was further purified using HPLC. The endo and exo products were separated. LC-MS: 514.3 [M+H]. LC/MS RT=2.17 and 2.238 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242981B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-f7d08102a7e743379bef537eb0edab05 |
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| Source note | uspto-grants-2016_01 |
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