HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluorophenyl isothiocyanate → 5-[(2-Fluorophenyl)amino]-N-[4-(propylsulfonyl)phenyl]-1,3,4-oxadiazole-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluorophenyl isothiocyanate | HCID 97520 | — |
| Reactant | 2-hydrazino-2-oxo-N-[4-(propylsulfonyl)phenyl]acetamide | HCID 59464171 | — |
| Reactant | HCID 178500682 | HCID 178500682 | — |
| Product | 5-[(2-Fluorophenyl)amino]-N-[4-(propylsulfonyl)phenyl]-1,3,4-oxadiazole-2-carboxamide | HCID 59464111 | — |
Reaction Steps
Following the general procedure of Example 105 but using 2-hydrazino-2-oxo-N-[4-(propylsulfonyl)phenyl]acetamide (Intermediate 97) as starting material in place of methyl [trans-4-(4-{[hydrazino(oxo)acetyl]amino}phenyl)cyclohexyl]acetate and using 2-fluorophenylisothiocyanate in place of 2-isothiocyanatopyridine the title compound was obtained as a solid; 1H NMR δ 0.90 (t, 3H), 1.46-1.62 (m, 2H), 3.18-3.27 (m, 2H), 7.12-7.20 (m, 1H), 7.22-7.35 (m, 2H), 7.87 (d, 2H), 7.99-8.10 (m, 3H), 10.90 (s, 1H), 11.50 (s, 1H); MS m/e MH+ 405.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795283B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-a2417397d7714bf5b50c7d2ae01e2585 |
| Source note | uspto-grants-2010_09 |