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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57584Generated: October 29, 2026

Diisopropylethylamine → Tert-butyl 3-((7-chloropyrido[3,4-b]pyrazin-5-ylamino)methyl)-3-fluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/57584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 3-(aminomethyl)-3-fluoropiperidine-1-carboxylateHCID 56973580—
Reactant5,7-Dichloropyrido(3,4-b)pyrazineHCID 71742827—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-((7-chloropyrido[3,4-b]pyrazin-5-ylamino)methyl)-3-fluoropiperidine-1-carboxylateHCID 8671737326.8%

Reaction Steps

tert-butyl 3-(aminomethyl)-3-fluoropiperidine-1-carboxylate (3.86 g, 16.6 mmol) and DIPEA (3.22 g, 24.9 mmol) were added to a solution of 5,7-dichloropyrido[3,4-b]pyrazine (3.32 g, 16.6 mmol) in THF (60 mL) and the mixture was refluxed overnight. The volatile components were evaporated and the residue was extracted with ethyl acetate. Ethyl acetate was washed with brine and dried. The solvent was removed in vacuo The crude residue was purified by silica-gel chromatography eluting with Hexane-50% EtOAc/Hexane (gradient) then C18 column to afford the subtitled compound as pale yellow solid 1.76 g. MS (m/z): 396 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434726B2
Source datasetuspto-grants-2016_09
ORD IDord-93a4037ccaae4252af2679660a6608b3
Source noteuspto-grants-2016_09