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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093714Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 178523488, compound

https://huagongshe.com/reaction/1093714

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 66545655HCID 66545655—
ReactantHCID 178525878HCID 178525878—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178523488HCID 17852348816.5%

Reaction Steps

DIPEA (232 mg, 1.8 mmol) was added to a stirred solution of [(5-phenyl-1H-pyrazole-3-carbonyl)-amino]-acetic acid (148 mg, 0.6 mmol) in DMF (2 mL) followed by HOBt (95 mg, 0.7 mmol) and EDCI.HCl (137 mg, 0.7 mmol. After 2 minutes (2,4-difluoro-phenyl)-piperidin-4-yl-amine dihydrochloride (prepared by the method used for the synthesis of Intermediate 3) (150 mg, 0.6 mmol) was added to the reaction mixture and stirring was continued at ambient temperature overnight. The reaction mixture was diluted with cold water, extracted with ethyl acetate and dried over sodium sulfate. The organic layer thus collected was concentrated under reduced pressure. Purification by column chromatography (using 60-120 silica gel and 5% MeoH in CHCl3 as eluent) to afford 43 mg (16.5% Yield) of 5-phenyl-1H-pyrazole-3-carboxylic acid {2-[4-(2,4-difluoro-phenylamino)-piperidin-1-yl]-2-oxo-ethyl}-amide. LC/MS [M+H]+: 440.18, 94.52%. 1H NMR (300 MHz, DMSO-d6): δ13.8 (s, 1H), 8.1 (m, 1H), 7.8 (m, 2H), 7.4 (m, 4H), 7.0 (m, 1H), 6.9 (m, 2H), 5.0 (m, 1H), 4.4 (m, 1H), 4.2 (m, 2H), 3.5 (m, 1H), 3.2 (m, 1H), 2.8 (m, 1H), 2.0 (m, 2H), 1.5 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-b3c8040ab48741fba2a1387d6376eaf6
Source noteuspto-grants-2012_03