HuagongsheHuagongshe Chemistry Print Report · For research reference only
N1-(pyridin-2-yl)benzene-1,2-diamine → HCID 22736654, 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-methylthiocinnamoyl chloride | HCID 22736701 | — |
| Product | HCID 22736654 | HCID 22736654 | — |
Reaction Steps
The titled compound was prepared from N-(2-pyridyl)-o-phenylenediamine and (E)-3-methylthiocinnamoyl chloride (Miller, R. D.; Reiser, O. J. Heterocycl. Chem. 1993, 30, 755) according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). MW: 343.46; mp: 139.6-140.6° C.; 1H-NMR (CDCl3) δ: 8.78 (1H, dd, J=5.1, 2.2 Hz), 8.00 (1H, ddd, J=7.7, 7.7, 2.2 Hz), 7.96 (1H, d, J=16.1 Hz), 7.83 (1H, d, J=7.3 Hz), 7.54-7.39 (5H, m), 7.38-7.18 (4H, m), 7.10 (1H, d, J=16.1 Hz), 2.49 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713482B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-590471c696274991b592646b1b528ce3 |
| Source note | uspto-grants-2004_03 |