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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469082Generated: October 29, 2026

Acetic Acid → N-{[4-({4-[(2-Aminopyridin-3-yl)methyl]piperazin-1-yl}carbonyl)-1,3-oxazol-2-yl]methyl}-N-cyclopropyl-4-methoxy-2,6-dimethylbenzenesulfonamide

https://huagongshe.com/reaction/469082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-Pyridinecarboxaldehyde, 2-amino-HCID 737633—
ReactantN-cyclopropyl-4-methoxy-2,6-dimethyl-N-{[4-(piperazin-1-ylcarbonyl)-1,3-oxazol-2-yl]methyl}benzenesulfonamideHCID 58392961—
Solvent1,2-DichloroethaneHCID 11—
ProductN-{[4-({4-[(2-Aminopyridin-3-yl)methyl]piperazin-1-yl}carbonyl)-1,3-oxazol-2-yl]methyl}-N-cyclopropyl-4-methoxy-2,6-dimethylbenzenesulfonamideHCID 58393415—

Reaction Steps

To a stirred solution of N-cyclopropyl-4-methoxy-2,6-dimethyl-N-{[4-(piperazin-1-ylcarbonyl)-1,3-oxazol-2-yl]methyl}benzenesulfonamide (30 mg, 0.07 mmol) in DCE (2 mL) were added 2-amino-3-pyridinecarboxaldehyde (10 mg, 0.08 mmol) and AcOH (3 μL, 0.07 mmol) and the reaction mixture was stirred for 1 h at ambient temperature. STAB (20 mg, 0.09 mmol) was added and the reaction was stirred for 16 h. The reaction mixture was quenched with H2O (2 mL) and extracted with DCM (3×2 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The resulting residue was purified using prep method D to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623859B2
Source datasetuspto-grants-2014_01
ORD IDord-ce16d11a81c74b368064c4b52cd5d55c
Source noteuspto-grants-2014_01