HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 24802949, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | HCID 59216810 | HCID 59216810 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 24802949 | HCID 24802949 | — |
Reaction Steps
The title compound was prepared according to general Method B using 4-Chloro-N-(5-chloro-2-hydrazinocarbonyl-pyridin-3-yl)-3-trifluoromethyl-benzenesulfonamide (100 mg, 0.234 mmol), trimethylorthoformate (80 mg, 0.75 mmol), acetonitrile (2 mL), 2-methylaniline (62 mg, 0.50 mmol) and acetic acid (1.0 mL). 1H NMR: (CD3OD, ppm): 8.82 (s, 1H), 8.40 (s, 1H), 8.27 (d, 1H), 8.05 (m, 1H), 7.75 (d, 1H), 7.61 (s, 1H), 7.39 (m, 1H), 7.32 (m, 1H), 7.25 (m, 2H), 2.15 (s, 3H). MS (ES) [M+H]+ expected 528.0. found 528.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445518B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-d957f855044a412fb4d7cb7712bad6e3 |
| Source note | uspto-grants-2013_05 |