HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-[3-(4-Cyano-phenyl)-6-nitro-indol-1-yl]-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(1-amino-6-nitro-1H-indol-3-yl)-benzonitrile | HCID 57442261 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[3-(4-Cyano-phenyl)-6-nitro-indol-1-yl]-acetamide | HCID 57442262 | 38% |
Reaction Steps
Add acetic anhydride (214 mg, 2.1 mmol) to a mixture of 4-(1-Amino-6-nitro-1H-indol-3-yl)-benzonitrile (400 mg, 1.4 mmol) and di-isopropylethylamine (194 mg, 2.1 mmol) and N,N-dimethylaminopyridine (2 mg) in DMF (20 mL) and stir for 3 h. Add additional acetic anhydride (214 mg, 2.1 mmol) and di-isopropylethylamine (194 mg, 2.1 mmol) and stir overnight. Dilute the mixture with water and extract with EtOAc. Wash the combined extracts with water and brine, and dry over MgSO4. Purify the crude residue using silica gel chromatography to give 170 mg (38% yield) of N-[3-(4-Cyano-phenyl)-6-nitro-indol-1-yl]-acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932284B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-6864b6321a7745a8b091e9ba25173e48 |
| Source note | uspto-grants-2011_04 |