HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Chloro-benzoic acid N'-(4-amino-3-nitro-benzoyl)-hydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chlorobenzohydrazide | HCID 10816 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Benzoic acid, 4-amino-3-nitro- | HCID 74115 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-benzoic acid N'-(4-amino-3-nitro-benzoyl)-hydrazide | HCID 46651557 | — |
Reaction Steps
To 4-Chloro-benzoic acid hydrazide (5.0 g, 29 mmol) and 4-Amino-3-nitro-benzoic acid (5.3 g, 29 mmol) in DMF (100 mL) was added HOBT (3.9 g, 29 mmol), and EDCI (5.5 g, 29 mmol), followed by triethylamine (12.1 mL, 87 mmol). The mixture was stirred at ambient temperature for 18 hours. Water (50 mL) was added to the reaction mixture. The precipitate was collected by filtration, washed with water, and dried under vacuum to provide the title compound as a yellow solid. 1H NMR(DMSO-d6, 400MHz) δ ppm 7.08 (d, J=8.97 Hz, 1 H) 7.61 (m, 2 H) 7.82-7.97 (m, 5 H) 8.66 (d,J=2.15 Hz, 1 H) 10.52 (s, 1 H) 10.57 (s, 1 H; (M+H)+=335.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08217065B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-9af772b74cf94eb085716ca95e56aeea |
| Source note | uspto-grants-2012_07 |