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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093734Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 178523511, compound

https://huagongshe.com/reaction/1093734

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Amino-1-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethanone hydrochlorideHCID 66591547—
ReactantHCID 178524124HCID 178524124—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178523511HCID 17852351151.7%

Reaction Steps

DIPEA (133 mg, 1.03 mmol) was added to a stirred solution of 5-(3-hydroxy-phenyl)-1H-pyrazole-3-carboxylic acid (60 mg, 0.294 mmol) (prepared from 5-(3-benzyloxy-phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester) in DMF (2 mL) followed by HOBt (41.7 mg, 0.308 mmol) and EDCI.HCl (59 mg, 0.308 mmol). After 2 minutes 2-amino-1-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethanone hydrochloride (prepared according to Step 1 and 5 of the General Scheme) (99 mg, 0.294 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 to afford the residue. Washing with ethyl acetate afforded 74 mg (51.7% Yield) of 5-(3-hydroxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-oxo-2-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethyl}-amide. LC/MS [M+H]+: 489, 96%. 1H NMR (300 MHz, DMSO-d6): δ13.6 (s, 1H), 9.6 (s, 1H), 8.0 (t, 1H), 7.5 (t, 1H), 7.1 (m, 7H), 6.9 (d, 1H), 6.8 (m, 1H), 4.8 (m, 1H), 4.2 (d, 2H), 3.9 (m, 1H), 3.7 (m, 1H), 3.4 (m, 2H), 2.0 (m, 2H), 1.6 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-6ca91a66769c4afab11152e3ad09defb
Source noteuspto-grants-2012_03