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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Bromo-o-fluorotolueneHCID 67968—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66807042HCID 66807042—
SolventDichloromethaneHCID 6344—
ProductHCID 56942350HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242981B2
Source datasetuspto-grants-2016_01
ORD IDord-f7d08102a7e743379bef537eb0edab05
Source noteuspto-grants-2016_01