Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093715Generated: November 1, 2026

1-Hydroxybenzotriazole → HCID 178523489, compound

https://huagongshe.com/reaction/1093715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 86634627HCID 86634627—
ReactantHCID 178525878HCID 178525878—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178523489HCID 17852348944.4%

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 (5-fluoro-2-trifluoromethyl-phenyl)-piperidin-4-yl-amine dihydrochloride (prepared according to 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 was concentrated under reduced pressure. Purification by column chromatography (using 60-120 silica gel and 5% MeoH in CHCl3 as eluent) afforded 129 mg (44.4% Yield) of 5-phenyl-1H-pyrazole-3-carboxylic acid {2-[4-(5-fluoro-2-trifluoromethyl-phenylamino)-piperidin-1-yl]-2-oxo-ethyl}-amide. LC/MS [M+H]+: 490.18, 95.08%. 1H NMR (300 MHz, DMSO-d6): δ13.8 (s, 1H), 8.0 (bs, 1H), 7.8 (d, 2H), 7.5 (t, 4H), 7.1 (bs, 1H), 6.8 (d, 1H), 6.5 (t, 1H), 5.0 (d, 1H), 4.4 (d, 1H), 4.3 (d, 2H), 3.8 (m, 2H), 3.7 (m, 2H), 3.2 (t, 1H), 2.8 (t, 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-5d473512a62645bbae3f65a3310a476e
Source noteuspto-grants-2012_03