HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenyl formate → N-methyl-N-(6-methyl-1H-indol-3-ylmethyl)-formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenyl formate | HCID 74628 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | methyl-(6-methyl-1H-indol-3-ylmethyl)-amine | HCID 68579797 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-methyl-N-(6-methyl-1H-indol-3-ylmethyl)-formamide | HCID 86619843 | — |
Reaction Steps
To a solution of crude methyl-(6-methyl-1H-indol-3-ylmethyl)-amine (87 mg) in acetonitrile (1 ml) was added diisopropylethyl amine (0.25 ml) and 4-nitrophenyl formate (90 mg) and stirring was continued for 3 h. The mixture was diluted with methanol and acetic acid evaporated and the residue was chromatographed on silica using n-heptane/AcOEt (1:1) to give N-methyl-N-(6-methyl-1H-indol-3-ylmethyl)-formamide as a colorless oil. MS: 202.9 ([M]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705034B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-f4a2a753db8f4fa19a40cda5259b2edb |
| Source note | uspto-grants-2010_04 |