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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556820Generated: October 25, 2026

Tetrahydro-2,5-dimethoxyfuran-3-carbaldehyde → tert-Butyl 3-((2-(5-cyanopyrazin-2-ylamino)-5-(3-formyl-1H-pyrrol-1-yl)pyridin-4-ylamino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/556820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydro-2,5-dimethoxyfuran-3-carbaldehydeHCID 567310—
ReactantTert-butyl 3-((5-amino-2-(5-cyanopyrazin-2-ylamino)pyridin-4-ylamino)methyl)piperidine-1-carboxylateHCID 66745373—
SolventDimethylformamide tolueneHCID 21735183—
Producttert-Butyl 3-((2-(5-cyanopyrazin-2-ylamino)-5-(3-formyl-1H-pyrrol-1-yl)pyridin-4-ylamino)methyl)piperidine-1-carboxylateHCID 86648387—

Reaction Conditions

Temperature80 °C

Reaction Steps

tert-Butyl 3-((5-amino-2-(5-cyanopyrazin-2-ylamino)pyridin-4-ylamino)methyl)piperidine-1-carboxylate (60 mg, 0.141 mmol) (Synthesis 101-C) was dissolved in DCE/AcOH (1/1, 5 mL). 2,5-Dimethoxytetrahydrofuran-3-carboxaldehyde (28 uL, 0.211 mmol) was added and the solution was stirred at 80° C. for 1 h. The solution was evaporated to dryness and the product (143 mg, approximately 50% purity) was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058045B2
Source datasetuspto-grants-2011_11
ORD IDord-4fd7608047874a25aea27a575e78ae29
Source noteuspto-grants-2011_11