HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenamine, 4-fluoro-N-(1-methylethyl)- → N-(4-fluorophenyl)-N-isopropyl-2-(2-propynyl)-N'-((E)-styrylsulfonyl)malonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenamine, 4-fluoro-N-(1-methylethyl)- | HCID 154403 | — |
| Reactant | (1E)-2-Phenylethenesulfonamide | HCID 5357731 | — |
| Reactant | N,N-diethyl-N'-(2-naphthylsulfonyl)-2-(2-propynyl)malonamide | HCID 86645224 | — |
| Product | N-(4-fluorophenyl)-N-isopropyl-2-(2-propynyl)-N'-((E)-styrylsulfonyl)malonamide | HCID 86645227 | 36.4% |
Reaction Steps
In the same manner as in Example 152 (3), the object compound was obtained using the compound (3.00 g) obtained in Example 152 (2) and trans-β-styrenesulfonamide (3.23 g). This was subjected to hydrolysis in the same manner as in Example 1 (3), and condensed with 4-fluoro-N-isopropylaniline (1.29 g) in the same manner as in Example 1 (4) to give a crude product. This was purified by silica gel column chromatography to give the title compound (1.25 g) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461209B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-64b9239aa5774de7b9aa6448f11cb14e |
| Source note | uspto-grants-2013_06 |