HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093732Generated: November 1, 2026
1-Hydroxybenzotriazole → HCID 178523505, compound
https://huagongshe.com/reaction/1093732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-Amino-1-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethanone hydrochloride | HCID 66591547 | — |
| Reactant | 3-(2-(trifluoromethyl)phenyl)-1H-pyrazole-5-carboxylic acid | HCID 178524112 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178523505 | HCID 178523505 | 56% |
Reaction Steps
DIPEA (76 mg, 0.59 mmol) was added to a stirred solution of 5-(2-trifluoromethyl-phenyl)-1H-pyrazole-3-carboxylic acid (43 mg, 0.167 mmol) (prepared by the method used for the synthesis of Intermediate 29, starting from (o-trifluoromethyl)acetophenone) in DMF (2 mL) followed by HOBt (24 mg, 0.176 mmol) and EDCI.HCl (34 mg, 0.176 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) (0.057 mg, 0.167 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. The residue was purified by washing with chloroform to afford 51 mg (56% Yield) of 5-(2-trifluoromethyl-phenyl)-1H-pyrazole-3-carboxylic acid {2-oxo-2-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethyl}-amide. LC/MS [M+H]+: 541, 87.52%. 1H NMR (300 MHz, DMSO-d6): δ13.8 (d, 1H), 8.1 (m, 1H), 7.6 (m, 4H), 7.5 (t, 1H), 7.3 (t, 3H), 6.76 (s, 1H), 4.8 (m, 1H), 4.1 (d, 2H), 3.7 (m, 2H), 3.4 (m, 1H), 3.2 (m, 1H), 1.9 (m, 2H), 1.6 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08129376B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-f2139c56c01544bb8061e511fdf4471a |
|---|
| Source note | uspto-grants-2012_03 |
|---|