HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397455Generated: October 30, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 67347720, compound
https://huagongshe.com/reaction/1397455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | N'-Hydroxybenzenecarboximidamide | HCID 69186 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67325165 | HCID 67325165 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67347720 | HCID 67347720 | 7% |
Reaction Steps
HOBt (47 mg, 0.35 mmol), EDCI (67 mg, 0.35 mmol), and diisopropylethylamine (0.7 mL, 1.0 mmol) were added to a solution of 3-(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamido)propanoic acid (115 mg, 0.35 mmol) and N′-hydroxybenzimidamide (47 mg, 0.35 mmol) in dichloromethane (3.5 mL) with a few drops of DMF. The reaction was stirred 1 h and then toluene was added and the reaction was heated to 90° C. for 1 h. The reaction was diluted with ethyl acetate and the organic layer was washed with saturated sodium bicarbonate and dried over sodium sulfate. The product was purified on reverse phase using water/acetonitrile to give N-(2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethyl)-3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide (10 mg, yield 7%). 1H NMR (CDCl3) δ 8.60 (s, 1H), 8.22 (m, 1H), 8.10 (m, 3H,) 7.60 (m, 1H), 7.55-7.45 (m, 3H), 4.05 (m, 2H), 3.26 (m, 2H). MS (ESI) m/z: Calculated for C20H14F3N5O3: 429.10. found: 430.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901156B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-e67b1c9cd0984f57a8078adc2c7828f8 |
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| Source note | uspto-grants-2014_12 |
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