HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 69462376, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | HCID 69463404 | HCID 69463404 | — |
| Product | HCID 69462376 | HCID 69462376 | 36% |
Reaction Steps
By replacing 5-(4-bromophenyl)-7,8-dimethoxy-1,3-dihydro-2H-1,4-benzodiazepin-2-one (XXIIaf) in example IIba by 3-benzyl-7,8-diethoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one (XXIIaj), and MeI by ethyl iodide, and proceeding in the same manner, the abovenamed product is obtained. Yield: 36%. M: 128–130° C. 1H-NMR (CDCl3, 200 MHz): d 1.10 (t, 3H, CH3), 1.40 (t, 3H, CH3), 1.55 (t, 3H, CH3), 3.66 (m, 3H, CH2Ph+CH), 3.94 (q, 2H, —OCH2), 4.15 (AB system, ? d=0.52, JAB=13.2, 2H, —NCH2), 4.19 (q, 2H, —OCH2), 6.67 (s, 1H Ar), 6.85 (s, 1H Ar), 7.33–7.63 (m, 10H Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250410B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-383a26b455c04166ad8163284c3a3de0 |
| Source note | uspto-grants-2007_07 |