HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → Benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | HCID 10755041 | HCID 10755041 | — |
| Product | Benzamide | HCID 2331 | 56.3% |
Reaction Steps
The title compound was synthesized as in Example 1 using p-anisidine (1.0 g, 7.1 mmol), CSI (0.85 mL, 9.8 mmol), and 3-amino-N-(3,4-difluoro-phenyl)-4-methoxy-benzamide (1.75 g, 6.3 mmol) to give 0.43 g of benzamide, N-(3,4-difluorophenyl)-4-methoxy-3-[[[[[(4-methoxyphenyl)amino]-carbonyl]amino]sulfonyl]amino]-. Microanalysis: C22H20F2N4O6S; calculated: C=52.17; H=3.98; N=11.06. found: C=52.17; H=3.89; N=10.95. Mp 189-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06906094B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-e20c99807d2b4d91a40fb64611e937b0 |
| Source note | uspto-grants-2005_06 |