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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241408Generated: October 31, 2026

Sodium Carbonate → Tert-butyl 4-[4-(6-amino-5-formylpyridin-3-yl)pyrazol-1-yl]-piperidine-1-carboxylate

https://huagongshe.com/reaction/241408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-5-iodopyridine-3-carbaldehydeHCID 17750177—
ReactantTert-butyl 4-[4-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)pyrazol-1-yl]piperidine-1-carboxylateHCID 67495092—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-[4-(6-amino-5-formylpyridin-3-yl)pyrazol-1-yl]-piperidine-1-carboxylateHCID 86664806—

Reaction Steps

150 mg (0.605 mmol) of 2-amino-5-iodopyridine-3-carbaldehyde and 413 mg (1.089 mmol) of tert-butyl 4-[4-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)pyrazol-1-yl]piperidine-1-carboxylate are dissolved in 2.3 ml of N,N-dimethylformamide in a nitrogen-filled microwave vessel, and 1.7 ml (3.4 mmol) of 2M sodium carbonate solution and 35 mg (0.030 mmol) of tetrakis(triphenylphosphine)palladium(0) are added. The reaction solution is irradiated with microwaves for 30 min at 120° C. in the Biotage SmithSynthesizer. The reaction mixture is cooled to room temperature and filtered. The filtrate is evaporated to dryness. The oily residue is purified by means of RP-HPLC, giving tert-butyl 4-[4-(6-amino-5-formylpyridin-3-yl)pyrazol-1-yl]-piperidine-1-carboxylate; HPLC-MS [M+H]+ 372.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648201B2
Source datasetuspto-grants-2014_02
ORD IDord-22780cbc61a64bfd8fb8086c92eba15a
Source noteuspto-grants-2014_02