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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093612Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 178425122, compound

https://huagongshe.com/reaction/1093612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(2,5-Dimethyl-phenyl)-piperidin-4-yl-amine dihydrochlorideHCID 66591423—
ReactantHCID 178525878HCID 178525878—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178425122HCID 17842512277.2%

Reaction Steps

To a stirred solution of [(5-phenyl-1H-pyrazole-3-carbonyl)-amino]-acetic acid (0.097 g, 0.00040 mol) in DMF (1 mL) was added DIPEA (0.233 g, 0.00180 mol), HOBt (0.053 g, 0.00040 mol) and EDCI.HCl (0.138 g, 0.00072 mol) at ambient temperature. After 2 minutes (2,5-dimethyl-phenyl)-piperidin-4-yl-amine dihydrochloride (0.1 g, 0.00036 mol) was added and the resulting mixture was stirred overnight. The reaction mixture was then diluted with cold water. The resulting precipitate was isolated by filtration and dried to afford 0.12 g (77%) of 5-phenyl-1H-pyrazole-3-carboxylic acid {2-[4-(2,5-dimethyl-phenylamino)-piperidin-1-yl]-2-oxo-ethyl}-amide. LCMS: 432.23 (M+1)+, 96.91%, 1H NMR (DMSO-d6): δ 8.1 (s, 1H), 7.8 (d, 2H), 7.5 (t, 2H), 7.4 (t, 1H), 7.1 (s, 1H), 6.8 (d, 1H), 6.5 (s, 1H), 6.3 (d, 1H), 4.4 (d, 2H), 4.2 (bs, 2H), 3.9 (d, 1H), 3.6 (bs, 1H), 3.2 (t, 1H), 2.8 (t, 1H), 2.2 (s, 3H), 2.0 (s, 3H), 1.9 (d, 1H), 1.5 (d, 1H), 1.3 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-7993a548539a402180da236f61e3c58c
Source noteuspto-grants-2012_03