HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Methoxybenzofuran-2-carboxylic acid → 5-methoxy-N-(5-methylhexan-3-yl)benzofuran-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Methoxybenzofuran-2-carboxylic acid | HCID 288638 | — |
| Reactant | 5-Methylhexan-3-amine | HCID 22955496 | — |
| Product | 5-methoxy-N-(5-methylhexan-3-yl)benzofuran-2-carboxamide | HCID 57527773 | 67% |
Reaction Steps
Prepared in a similar manner to example 4 using 5-methoxybenzofuran-2-carboxylic acid and 5-methylhexan-3-amine (example 5a). Yield: 67%. 1H NMR (500 MHz, CDCl3): δ 0.96 (m, 9H); 1.39-1.52 (m, 3H); 1.66 (m, 2H); 3.85 (s, 3H); 4.17 (m, 1H); 6.24 (d, 1H); 7.01 (dd, 1H); 7.08 (d, 1H); 7.38 (m, 2H). MS (290, M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124121B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-1d8ce9bb29be4f04aca5184aa9ce83ac |
| Source note | uspto-grants-2012_02 |