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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068772Generated: November 1, 2026

Trityl chloride → HCID 86647616, compound

https://huagongshe.com/reaction/2068772

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 numberUS08299057B2
Source datasetuspto-grants-2012_10
ORD IDord-b03cb2babe9d4925bcd0d06c01dc3570
Source noteuspto-grants-2012_10