HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetanilide → HCID 24821528, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetanilide | HCID 904 | — |
| Reactant | 2-Bromo-6-methyl-3-nitropyridine | HCID 24728013 | — |
| Product | HCID 24821528 | HCID 24821528 | 51.1% |
Reaction Steps
The title compound was prepared with the analogous procedure described in example 3 using 2-Bromo-6-methyl-3-nitropyridine (108 mg, 0.5 mmol) and N-phenylacetamide (81 mg, 0.6 mmol) as starting materials to yield the title compound as brown viscous oil (57 mg, 51%). 1H NMR (DMSO) δ 2.42 (s, 3 H), 3.31 (s, 3 H), 7.11 (d, J=8.0 Hz, 1 H), 7.51-7.63 (m, 5 H), 7.89 (d, J=8.0 Hz, 1 H); 13C NMR δ 14.6, 23.8, 118.0, 126.1, 127.7, 128.7, 129.4, 132.1, 134.8, 148.3, 150.9, 151.1. HRMS: cal for C14H14N3 [M+H+]: 224.1188; found: 224.1184.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735586B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-c16a2c1065054da1b1053edc9c4d2a1f |
| Source note | uspto-grants-2014_05 |