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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093676Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 57874394, compound

https://huagongshe.com/reaction/1093676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-biphenyl-4-yl-malonamic acidHCID 55049154—
Reactant(2,5-Dimethyl-phenyl)-piperidin-4-yl-amine dihydrochlorideHCID 66591423—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57874394HCID 5787439416%

Reaction Steps

To a stirred solution of N-biphenyl-4-yl-malonamic acid (0.101 g, 0.00039 mole) in DMF (1 mL) was added DIPEA (0.233 g, 0.0018 mole), HOBt (0.053 g, 0.00039 mole) and EDCI.HCl (0.138 g, 0.00072 μmole). After 2 minutes (2,5-dimethyl-phenyl)-piperidin-4-yl-amine dihydrochloride (0.101 g, 0.00039 mole) was added and the resulting mixture was stirred overnight. The reaction mixture was then diluted with cold water and the resulting precipitate was isolated by filtration. Purification by column chromatography using silica gel 60-120 mesh (1% methanol in chloroform) afforded 0.025 g (16%) of N-biphenyl-4-yl-3-[4-(2,5-dimethyl-phenylamino)-piperidin-1-yl]-3-oxo-propionamide. LC-MS purity: 442.24 (M+1)+, 97.08%, 1H NMR (DMSO-d6): δ 10.1 (s, 1H), 7.7-7.5 (m, 6H), 7.4 (t, 2H), 7.35 (d, 1H), 6.9 (d, 1H), 6.5 (t, 2H), 4.5 (d, 1H), 4.0 (d, 1H), 3.7 (s, 1H), 3.5 (s, 2H), 3.4 (t, 2H), 3.1 (t, 1H), 2.3 (s, 3H), 2.2 (d, 2H), 2.1 (s, 3H), 1.5 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-63e3c7911ab94a9bbc1b0e76e113409a
Source noteuspto-grants-2012_03