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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527277Generated: October 27, 2026

4,5,6,7-Tetrafluoro-1H-indole-3-carbaldehyde → HCID 178513724, compound

https://huagongshe.com/reaction/527277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,5,6,7-Tetrafluoro-1H-indole-3-carbaldehydeHCID 2776702—
ReactantSodium borohydrideHCID 4311764—
Reactant5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamideHCID 86698956—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 178513724HCID 178513724—

Reaction Steps

5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamide (100 mg) was then suspended in EtOH (4 mL) and 4,5,6,7-tetrafluoro-1H-indole-3-carbaldehyde (1 eq.) and piperidine (1 drop) were added. Stirred at reflux until intermediate was absent (HPLC). After reaction was complete (18 hrs) it was brought to room temperature and filtered to obtain product as a yellow powder. Powder was washed with EtOH. Product was allowed to dry under vacuum for 1 hr. Resulting imine was suspended in 5 mL MeOH and sodium borohydride (3 eq.) was added. HPLC confirmed reaction was complete (absence of imine). After completion (1 hr), precipitate was filtered to obtain D22 as a light yellow powder as product. Product was washed with deionized water to remove excess sodium borohydride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346792B2
Source datasetuspto-grants-2016_05
ORD IDord-d652ca67d388432f8c3de5d568093a7a
Source noteuspto-grants-2016_05