HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093788Generated: November 2, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 57874452, compound
https://huagongshe.com/reaction/1093788
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 3-Aminobenzonitrile | HCID 16702 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-1-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethanone hydrochloride | HCID 66591547 | — |
| Reactant | 1-(3-cyano-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid | HCID 66591603 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57874452 | HCID 57874452 | 16% |
Reaction Steps
DIPEA (61 mg, 4.7 mmol) was added to a stirred solution of 1-(3-cyano-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid (202 mg, 0.94 mmol) (prepared by the method used for the synthesis of Intermediate 64, starting from 3-aminobenzonitrile) in DMF (5 mL) followed by HOBt (14 mg, 1.03 mmol) and EDCI (452 mg, 2.36 mmol). After 2 minutes of stirring, 2-amino-1-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethanone hydrochloride (prepared according to Step 1 and 5 of the General Scheme) (351 mg, 1.03 mmol) was added and the resulting mixture was stirred at ambient temperature overnight. Cold water was then added and the solid was collected. The solid obtained was purified by column chromatography (using 60-120 silica gel and 30-70% EtOAc in hexane as eluent) to afford 75 mg (16% Yield) of 1-(2-cyano-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid {2-oxo-2-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethyl}-amide. LC/MS [M+H]+: 499, 99.08%. 1H NMR (300 MHz, DMSO-d6): δ 9.48 (s, 1H), 8.58 (t, 2H), 8.4 (d, 1H), 8.06 (d, 1H), 7.9 (t, 1H), 7.38 (t, 3H), 4.9 (m, 1H), 4.3 (d, 2H), 4.0 (s, 1H), 3.8 (s, 1H), 3.5 (m, 2H), 2.1 (t, 2H), 1.8 (s, 1H), 1.6 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129376B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-a9372ba5f02c44a7b9f63e8987a828e3 |
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| Source note | uspto-grants-2012_03 |
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