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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512944Generated: October 30, 2026

Trityl chloride → HCID 86647616, compound

https://huagongshe.com/reaction/512944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 86647615HCID 86647615—
SolventDichloromethaneHCID 6344—
ProductHCID 86647616HCID 8664761640%

Reaction Conditions

Temperature0 °C

Reaction Steps

Crude N-[5-(3,5-difluoro-benzyl)-1H-indazol-3-yl]-2,2,2-trifluoro-acetamide was suspended in dichloromethane (25 mL) and treated with trityl chloride (0.72 g, 2.58 mmol) under stirring. The suspension was cooled to 0° C. and neat 1,8-diazabicyclo[5.4.0]undec-7-ene (0.42 mL, 2.78 mmol) was added, producing immediate solubilization. After stirring at 0° C. for 3 hours the reaction mixture was poured into 50 mL of ice containing 1N HCl (5 mL) and extracted with dichloromethane. The organic layer was washed with NaHCO3, brine, dried and concentrated to a crude material that was purified by flash chromatography (eluant: DCM). The desired product was obtained as a white solid (450 mg, yield 40% over two steps)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102662B2
Source datasetuspto-grants-2015_08
ORD IDord-584a75c5da574572b88df55f7aaea2e0
Source noteuspto-grants-2015_08