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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405119Generated: November 2, 2026

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

https://huagongshe.com/reaction/1405119

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 numberUS08916555B2
Source datasetuspto-grants-2014_12
ORD IDord-8377b424346a443ba0b52b9be3fef25c
Source noteuspto-grants-2014_12