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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093695Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 57874420, compound

https://huagongshe.com/reaction/1093695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-(6-phenyl-pyridin-3-yl)-malonamic acidHCID 57874490—
ReactantHCID 86634622HCID 86634622—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57874420HCID 5787442067%

Reaction Steps

To a stirred solution of N-(6-phenyl-pyridin-3-yl)-malonamic acid (0.07 g, 0.00024 mole) in DMF (1 mL) was added DIPEA (0.153 g, 0.00120 mole), HOBt (0.039 g, 0.000286 mole) and EDCI.HCl (0.055 g, 0.00029 mole). After 2 minutes (2-trifluoromethyl-phenylsulfanyl)-piperidin-4-yl-amine hydrochloride (0.085 g, 0.00029 mole) was added and the resulting mixture was stirred overnight. The reaction mixture was then diluted with cold water and the product was extracted with ethyl acetate. The organic layer was washed with brine solution, dried over sodium sulfate and concentrated under reduced pressure to afford 80.2 mg (67%) of 3-oxo-N-(6-phenyl-pyridin-3-yl)-3-[4-(2-trifluoromethyl-phenylsulfanyl)-piperidin-1-yl]-propionamide. LC-MS purity: 501.15 (M+1)+, 95.38%, 1H NMR (DMSO-d6): δ 10.5 (s, 1H), 8.8 (d, 1H), 8.2 (d, 1H), 8.1 (d, 2H), 8.0 (d, 1H), 7.7 (d, 1H), 7.6-7.4 (m, 5H), 7.2 (t, 1H), 4.3 (d, 1H), 3.9 (d, 1H), 3.7-3.6 (m, 3H), 3.3-3.2 (m, 1H), 3.0 (m, 1H), 2.0 (m, 2H), 1.7-1.6 (m, 1H), 1.5-1.4 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-1d390b7c7adf4f0bb8572ed7c7ab46e5
Source noteuspto-grants-2012_03