HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 178517580, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 86645368 | HCID 86645368 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178517580 | HCID 178517580 | — |
Reaction Conditions
| Temperature | 220 °C |
|---|
Reaction Steps
To a solution of 2-(3-(4-(4-chlorophenoxy)phenyl)-2-oxo-4-(3-(trifluoromethyl)phenyl)-imidazolidin-1-yl)acetonitrile (21.8 mg, 0.046 mmol) in DMF (1.0 mL) are added NaN3 (60 mg, 0.92 mmol) and NH4Cl (49 mg, 0.92 mmol). The reaction mixture is heated at 220° C. for 15 min in a microwave reactor. After cooling down to room temperature and removal of the solvent, the residue is purified by preparatory LC/MS to provide the title compound; 1H NMR (CDCl3, 400 MHz) δ 7.58-7.45 (m, 4H), 7.26 (d, 2H), 7.19 (d, 2H), 6.87 (m, 4H), 5.24 (dd, 1H), 4.95 (d, 1H), 4.69 (d, 1H), 4.10 (t, 1H), 3.48 (dd, 1H); HPLC-MS calculated for C24H18ClF3N6O2 (M+H+) 515.1, found 515.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431607B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-ac0aceef3f4941bbba3f297702288fb6 |
| Source note | uspto-grants-2013_04 |