HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-phenyl-1,3,4-thiadiazole → 2-Methyl-6-(thieno[3,2-b]pyridin-7-yloxy)-benzofuran-3-carboxylic acid (5-phenyl-[1,3,4]thiadiazol-2-yl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-phenyl-1,3,4-thiadiazole | HCID 219408 | — |
| Reactant | 2-Methyl-6-[thieno[3,2-b]pyridin-7-yloxy]benzofuran-3-carboxylic acid | HCID 22143510 | — |
| Product | 2-Methyl-6-(thieno[3,2-b]pyridin-7-yloxy)-benzofuran-3-carboxylic acid (5-phenyl-[1,3,4]thiadiazol-2-yl)-amide | HCID 20767812 | — |
Reaction Steps
This material was prepared from 2-methyl-6-[thieno[3,2-b]pyridin-7-yloxy]benzofuran-3-carboxylic acid 100 and 5-phenyl-[1,3,4]thiadiazol-2-ylamine in a similar manner as that described for example 102. 1H NMR (CD3CN/CD3OD) δ8.45 (1H, d, J=5.6 Hz), 8.00-7.95 (4H, m), 7.52-7.50 (4H, m), 7.48 (1H, d, J=2.3 Hz), 7.25 (1H, dd, J=8.6, 2.3 Hz), 6.66 (1H, d, J=5.3 Hz), 2.76 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06869962B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-ea0045f874424b02a789faaedbab22ff |
| Source note | uspto-grants-2005_03 |