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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093694Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 57874492, compound

https://huagongshe.com/reaction/1093694

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 86634620HCID 86634620—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57874492HCID 5787449260%

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, 0.00029 mole) and EDCI.HCl (0.055 g, 0.00029 mole). After 2 minutes (2-bromo-phenylsulfanyl)-piperidin-4-yl-amine hydrochloride (0.088 g, 0.00028 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 73.2 mg (60%) of 3-[4-(2-bromo-phenylsulfanyl)-piperidin-1-yl]-3-oxo-N-(6-phenyl-pyridin-3-yl)-propionamide. LC-MS purity: 510.08 (M+1)+, 93.64%, 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), 7.84-7.7 (m, 2H), 7.7 (t, 1H), 7.54-7.36 (m, 4H), 4.3 (d, 1H), 3.9 (d, 1H), 3.8-3.7 (m, 1H), 3.6 (s, 2H), 3.3-3.2 (m, 1H), 3.0-2.9 (m, 1H), 2.0 (t, 2H), 1.6-1.5 (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-c2dc97d59fdf4a9980b728ac33c8c7f6
Source noteuspto-grants-2012_03