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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952167Generated: October 30, 2026

Potassium Hydroxide → (5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-[2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazol-3-yl]-methanone

https://huagongshe.com/reaction/1952167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant5-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 24229213—
Reactant2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carbaldehydeHCID 57619207—
SolventMethanolHCID 887—
Product(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-[2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazol-3-yl]-methanoneHCID 249542842.1%

Reaction Steps

5-Chloro-1H-pyrrolo[2,3-b]pyridine (532, 0.068 g, 0.44 mmol) was combined with methanol (10 mL) and potassium hydroxide (0.16 g, 2.8 mmol). The mixture was stirred for 50 minutes, then 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carbaldehyde (530, 0.100 g, 0.40 mmol, prepared as described in Example 47, Scheme 162, Step 5) was added and the reaction was stirred overnight at room temperature and then concentrated. Ethyl acetate was added and the mixture was washed with sodium bicarbonate saturated solution and brine. After drying over anhydrous sodium sulfate the solvent was removed under reduced pressure. Purification with silica gel column chromatography eluting with a gradient of ethyl acetate (10-100%) in hexanes provided the desired compound (0.0033 g, 2%). MS (ESI) [M+H+]+=398.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404700B2
Source datasetuspto-grants-2013_03
ORD IDord-1946e50d80c641689f139e916b06d4d4
Source noteuspto-grants-2013_03