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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665631Generated: October 30, 2026

5-Amino-2,3-dihydro-1,3-benzoxazol-2-one → HCID 44231327, compound

https://huagongshe.com/reaction/1665631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2,3-dihydro-1,3-benzoxazol-2-oneHCID 26856—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionic acidHCID 57875811—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 44231327HCID 4423132732%

Reaction Conditions

Temperature10 °C

Reaction Steps

HOBt (72 mg, 0.53 mmol) and DMAP (81 mg, 0.66 mmol) were added to a stirred solution of 3-oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionic acid (150 mg, 0.44 mmol) in DMF (2 mL). The reaction mixture was cooled to 10° C. and EDCI.HCl (102 mg, 0.53 mmol) followed by 5-amino-3H-benzooxazol-2-one (66 mg, 0.44 mmol) were added. The reaction mixture was stirred at room temperature overnight then diluted with water and the product extracted with ethyl acetate. The ethyl acetate was washed with brine solution, dried over Na2SO4 and concentrated. The residue was purified by column chromatography using silica gel 60-120 mesh (90% ethyl acetate in hexane) to afford 65 mg (32%) of 3-oxo-N-(2-oxo-2,3-dihydro-benzooxazol-5-yl)-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionamide. LCMS: 477.12 (M+1)+, 96.35%, 1H NMR: (DMSO-d6): δ 11.6 (s, 1H), 10.2 (d, 1H), 7.8 (q, 2H), 7.6 (m, 3H), 7.22 (m, 1H), 7.08 (t, 1H), 3.74 (m, 1H), 3.6 (s, 2H), 3.52 (s, 1H), 3.32 (s, 1H), 3.16 (m. 1H), 3.8 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039463B2
Source datasetuspto-grants-2011_10
ORD IDord-6ba55774a84247759fba6b5471b231a1
Source noteuspto-grants-2011_10