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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177966Generated: November 1, 2026

1-Hydroxybenzotriazole → HCID 25164724, compound

https://huagongshe.com/reaction/1177966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Phenylnicotinic acidHCID 120118—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA saltHCID 86634088—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 25164724HCID 2516472470.7%

Reaction Steps

DIPEA (77 mg, 0.6 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt (103 mg, 0.24 mmol) in DMF (1 mL). HOBT (33 mg, 0.24 mmol) and EDCI.HCl (46 mg, 0.24 mmol) were then added at room temperature. After 2 minutes, 6-phenyl nicotinic acid (40 mg, 0.2 mmol) was added and the resulting mixture was stirred at room temperature for 4 hrs. Cold water was then added and the product was extracted with EtOAc and the organic layer was washed with brine. The organic phase was dried over Na2SO4 and concentrated under reduced pressure to afford 70 mg (70.7% yield) of N-{2-Oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-6-phenyl-nicotinamide. LCMS Purity: 92.6%, 1H NMR (DMSO-d6): δ 9.1 (s, 1H), 8.7 (t, 1H), 8.3 (d, 1H), 8.2-8.1 (m, 3H), 7.9-7.7 (m, 3H), 7.7-7.6 (m, 1H), 7.6-7.4 (m, 4H), 4.2 (m, 2H), 3.4-3.2 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-9687cdac11544f13a281abacccff2a5a
Source noteuspto-grants-2010_11