HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 57642253, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 68839571 | HCID 68839571 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 57642253 | HCID 57642253 | — |
Reaction Steps
N-(3-Chloromethyl-phenyl)-2-[5-cyclohexyl-1-(3,3-dimethyl-2-oxo-butyl)-2-oxo-1,2-dihydro-3H-1,3,4-benzotriazepin-3-yl]-acetamide (Example 49, step a) (52 mg, 0.0 mmol) was reacted with thiourea (7.6 mg, 0.0 mmol) and NaI (2 mg) in refluxing acetone (10 ml) for 3 h. After cooling, the solvents were concentrated in vacuo, affording the title compound as a yellow solid after trituration with Et2O (18 mg, 30%). 1H NMR (DMSO-d6) 9.89 (1H, br s), 8.99 (3H, br s), 7.75-7.46 (3H, m), 7.29-7.04 (5H, m), 4.77 (2H, m), 4.40 (2H, m), 4.38 (1H, m), 3.93 (1H, m), 2.86 (1H, m), 1.73-1.64 (6H, m), 1.21-1.08 (13H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524837B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-75f60dca666148d1a2d1ec48bf33cc48 |
| Source note | uspto-grants-2009_04 |