HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-benzyl-8-ethoxy-1-ethyl-7-methoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | HCID 69461618 | HCID 69461618 | — |
| Product | 3-benzyl-8-ethoxy-1-ethyl-7-methoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one | HCID 69458879 | 65% |
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-8-ethoxy-7-methoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one (XXIIbb), and methyl iodide by ethyl iodide, and proceeding in the same manner, the abovenamed product is obtained. Yield: 65%. F: 228–230° C. 1H-NMR (CDCl3, 300 MHz): d 1.03–1.08 (m, 3H, NCH2CH3), 1.50–1.54 (m, 3H, OCH2CH3), 3.59–3.65 (m, 3H, 1HNCH2+CH2Bn), 3.70 (s, 3H, OCH3), 3.77–3.83 (m, 1H, 1CH), 4.12–4.18 (m, 2H, OCH2), 4.30–4.41 (m, 1H, 1HNCH2), 6.62 (s, 1H Ar), 6.79 (s, 1H Ar), 7.22–7.59 (m, 10H Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250410B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-d1af6bd00a8c4d1eab08b447453164c5 |
| Source note | uspto-grants-2007_07 |