HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetanilide → HCID 24821451, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetanilide | HCID 904 | — |
| Reactant | 3-Bromo-2-nitropyridine | HCID 594044 | — |
| Product | HCID 24821451 | HCID 24821451 | 47% |
Reaction Steps
The title compound was prepared with the analogous procedure described in example 3 using 3-Bromo-2-nitropyridine (101 mg, 0.5 mmol) and N-phenylacetamide (81 mg, 0.6 mmol) as starting materials to yield the title compound as brown viscous oil (49 mg, 47% yield). 1H NMR (DMSO) δ 2.54 (s, 3 H), 7.35-7.68 (m, 6 H), 7.77 (d, J=8.8 Hz, 1 H), 8.58 (br s, 1 H); 13C NMR δ 14.0, 118.9, 120.1, 126.8, 128.5, 129.6, 130.1, 133.9, 143.0, 151.6, 156.7. HRMS (FAB): cal. for C13H12N3 [M-FH+]: 210.1031; found: 210.1026.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735586B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-31b09b37a8c14224bf3abe50b5174384 |
| Source note | uspto-grants-2014_05 |