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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056353Generated: November 4, 2026

Ethanol → 3-{(3r,4r)-4-Methyl-3-[methyl(1h-pyrrolo[2,3-b]pyridin-4-yl)amino]piperidin-1-yl}-3-oxopropanenitrile

https://huagongshe.com/reaction/2056353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2,5-Dioxopyrrolidin-1-yl 2-cyanoacetateHCID 53415896—
ReactantN-methyl-N-[(3R,4R)-4-methylpiperidin-3-yl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-amineHCID 66662875—
Product3-{(3r,4r)-4-Methyl-3-[methyl(1h-pyrrolo[2,3-b]pyridin-4-yl)amino]piperidin-1-yl}-3-oxopropanenitrileHCID 11522475182.5%

Reaction Steps

A mixture of N-methyl-N-[(3R,4R)-4-methylpiperidin-3-yl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-amine (43.0 mg, 0.000176 mol) and 3-[(2,5-dioxopyrrolidin-1-yl)oxy]-3-oxopropanenitrile (38 mg, 0.00021 mol) in ethanol (1 mL, 0.02 mol) was stirred overnight. The reaction mixture was partitioned between ethyl acetate/THF and sat. NaHCO3, and the organic layer was washed by sat. NaCl. The solvent was removed under vacuum to give 100 mg of an orange solid which was chromatographed with 7% MeOH/DCM, 0.7% NH4OH to give 17 mg of pale orange solid. The crude product was triturated with Et2O and the resulting solid was filtered and washed to give 9.4 mg of wet pale orange solid which was dried at from room temperature to about 60° C. for 3.5 h to give 6.5 mg of the final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335667B2
Source datasetuspto-grants-2008_02
ORD IDord-ee595da275ed4ecc8422222d337333c6
Source noteuspto-grants-2008_02