HuagongsheHuagongshe Chemistry Print Report · For research reference only
N1-(pyridin-2-yl)benzene-1,2-diamine → HCID 22736724, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N1-(pyridin-2-yl)benzene-1,2-diamine | HCID 752150 | — |
| Reactant | (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole | HCID 9796241 | — |
| Reactant | (E)-3-methoxycinnamoyl chloride | HCID 11367603 | — |
| Product | HCID 22736724 | HCID 22736724 | — |
Reaction Steps
The titled compound was prepared from N-(2-pyridyl)-o-phenylenediamine and (E)-3-methoxycinnamoyl chloride (Wiesler, W. T.; Nakanishi, K. J. Am. Chem. Soc., 1990, 112, 5574) according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). MW: 327.39; mp: 145.5-146.5° C.; 1H-NMR (CDCl3) δ: 8.81-8.76 (1H, m), 8.04-7.96 (1H, m), 7.98 (1H, d, J=16.1 Hz), 7.85-7.79 (1H, m), 7.56-7.41 (5H, m), 7.37-7.22 (3H, m), 7.00 (1H, d, J=16.1 Hz), 6.88 (1H, d, J=8.4 Hz), 3.83 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713482B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-7fbb027c788a4b32ae891c0077233e05 |
| Source note | uspto-grants-2004_03 |