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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531669Generated: October 30, 2026

Sodium Carbonate → tert-butyl 4-(3-(3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)benzyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/531669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-(3-fluorobenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 69132726—
Reactanttert-butyl 4-(3-(3-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)benzyl)piperidine-1-carboxylateHCID 90064887—
CatalystHCID 178477754HCID 178477754—
SolventEthanol toluene waterHCID 86587398—
Producttert-butyl 4-(3-(3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)benzyl)piperidine-1-carboxylateHCID 9003125663.1%

Reaction Steps

Using similar reaction conditions as described in step-i of example-1, tert-butyl 4-(3-(3-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)benzyl)piperidine-1-carboxylate (intermediate 66G) (300 mg, 0.44 mmol) was coupled with 1-(3-fluorobenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (intermediate 11) (170 mg, 0.58 mmol) using Pd(DPPF)Cl2 (15 mg, 0.02 mmol) and sodium carbonate (140 mg, 1.32 mmol) in toluene/ethanol/water (15/8/4 ml) to afford 200 mg (62.3% yield) of the titled compound after column purification using 30% ethyl acetate in hexane as eluent. MS: m/z=720.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353107B2
Source datasetuspto-grants-2016_05
ORD IDord-0bf338e9ffa24e17b8258f92b5dfe220
Source noteuspto-grants-2016_05