HuagongsheHuagongshe Chemistry Print Report · For research reference only
N1-(pyridin-2-yl)benzene-1,2-diamine → HCID 22736753, 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 | (2E)-3-(furan-2-yl)prop-2-enoyl chloride | HCID 10920765 | — |
| Product | HCID 22736753 | HCID 22736753 | — |
Reaction Steps
The titled compound was prepared from N-(2-pyridyl)-o-phenylenediamine and (E)-3-(2-furyl)acryloyl chloride (New, J. S.; Christopher, W. L.; Yevich, J. P.; Butler, R.; Schlemmer, R. F.; VanderMaelen, C. P.; Cipollina, J. A. J. Med. Chem., 1989, 32, 1147) according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). MW: 287.32; mp: 164.0-165.0° C.; 1H-NMR (CDCl3) δ: 8.80-8.75 (1H, m), 8.00 (1H, ddd, J=7.7, 7.7, 1.8 Hz), 7.83-7.78 (1H, m), 7.78 (1H, d, J=15.4 Hz), 7.54-7.39 (4H, m), 7.37-7.16 (2H, m), 7.01 (1H, d, J=15.4 Hz), 6.51 (1H, d, J=3.3 Hz), 6.44 (1H, dd, J=3.3, 1.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713482B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-ca879f38964b4a91a58774b8d9e54a72 |
| Source note | uspto-grants-2004_03 |