Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177972Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 25164925, compound

https://huagongshe.com/reaction/1177972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-phenylpyridine-2-carboxylic AcidHCID 2762870—
Reactant2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA saltHCID 86634088—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 25164925HCID 2516492573.3%

Reaction Steps

DIPEA (59 mg, 0.45 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt. (78 mg, 0.18 mmol) in DMF (1 mL). HOBT (24 mg, 0.18 mmol) and EDCI.HCl (29 mg, 0.15 mmol) were then added at room temperature. After 2 minutes, 5-phenyl-pyridine-2-carboxylic acid (30 mg, 0.15 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 55 mg (73.3% yield) of 5-phenyl-pyridine-2-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide LCMS Purity %: 90.8%, 1H NMR (DMSO-d6): δ 9.0 (d, 1H), 8.9-8.8 (t, 1H), 8.3 (dd, 1H), 8.1 (m, 1H), 7.9-7.6 (m, 5H), 7.6-7.4 (m, 4H), 4.4-4.3 (d, 1H), 4.2 (d, 1H), 3.8-3.4 (m, 6H), 3.2-3.1 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-e14c9a88b92643e0b65ffd4f1d17fc2e
Source noteuspto-grants-2010_11