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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410448Generated: November 1, 2026

Formate → HCID 59587370, compound

https://huagongshe.com/reaction/1410448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormateHCID 283—
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 59587593HCID 59587593—
SolventDichloromethaneHCID 6344—
ProductHCID 59587370HCID 5958737050%

Reaction Steps

To a solution of tert-butyl 4-(4-(4-carbamoyl-2-(2,6-difluorophenyl)oxazol-5-yl)benzyl)piperazine-1-carboxylate (0.100 g, 0.2 mmol) in DCM (3 mL) was added 4M HCl in dioxane (2 mL, 8.0 mmol) and the resulting mixture stirred at room temperature overnight. The solvent was removed in vacuo. The residue was purified by preparative HPLC to afford 2-(2,6-difluorophenyl)-5-(4-(piperazin-1-ylmethyl)phenyl)oxazole-4-carboxamide (0.043 g, 0.1 mmol, 50%) as a white solid as the formate salt. 1H NMR (DMSO) 2.44 (4H, m), 2.88 (4H, m), 3.55 (2H, s), 7.40 (2H, t), 7.47 (2H, d), 7.75 (3H, m), 8.19 (2H, d), 8.32 (1H, s). LCMS (2) Rt: 2.63 min; m/z (ES+) 399.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921544B2
Source datasetuspto-grants-2014_12
ORD IDord-ea7465538c57447fa6c72f03580e02b6
Source noteuspto-grants-2014_12