HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 17922784, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | HCID 22291112 | HCID 22291112 | — |
| Product | HCID 17922784 | HCID 17922784 | 64% |
Reaction Steps
Using an analogous procedure to that described in Example 61, N-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-methanesulphonylaminobenzamide was reacted with ethyl iodide to give the title compound in 64% yield; m.p. 192-193° C.; NMR Spectrum: (DMSOd6) 1.05 (t, 3H), 2.21 (s, 3H), 3.16 (t, 4H), 3.73 (m, 6H), 7.13 (m, 1H), 7.23 (d, 1H), 7.36 (m, 2H), 7.43 (d, 1H), 7.58 (m, 3H), 7.81 (d, 1H), 7.95 (m, 2H), 7.99 (d, 1H), 10.0 (s, 1H), 10.12 (s, 1H); Mass Spectrum: M+H+ 537.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956037B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-90dc39372ac9428aa05e120b8458d49e |
| Source note | uspto-grants-2005_10 |