HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Diamino-4,5-difluorobenzene → HCID 135839327, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Diamino-4,5-difluorobenzene | HCID 2736755 | — |
| Reactant | 319474-36-7 | HCID 135839310 | — |
| Reactant | HCID 178520042 | HCID 178520042 | — |
| Product | HCID 135839327 | HCID 135839327 | — |
Reaction Steps
Using the same procedure as for the synthesis of 3-(1H-benzoimidazol-2-yl)-1H-indazole-6-carboxylic acid in Example 53(a), step (ii), N-(4-hydroxyphenyl)-3-formyl-1H-indazole-6-carboxamide and 4,5-difluoro-1,2-phenylenediamine gave 3-(5,6-difluoro-1H-benzoimidazol-2-yl)-N-(4-hydroxyphenyl)-1H-indazole-6-carboxamide as a tan solid. 1H NMR (DMSO-d6) δ 13.99 (1H, s), 13.27 (1H, s), 10.21 (1H, s), 9.25 (1H, s), 8.52 (1H, d, J=8.7 Hz), 8.21 (1H, s), 7.85 (1H, d, J=9.0 Hz), 7.80 (1H, t, J=9.8 Hz), 7.55 (2H, d, J=8.7 Hz), 7.47 (1H, t, J=9.8 Hz), 6.75 (2H, d, J=8.7 Hz). MS (APCI positive) 406.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06891044B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-3f297aca845744a4b14d3f9a7bb8c38c |
| Source note | uspto-grants-2005_05 |