HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[bis(methylsulfanyl)methylidene]methanesulfonamide → HCID 178504234, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[bis(methylsulfanyl)methylidene]methanesulfonamide | HCID 13449843 | — |
| Reactant | 4-Cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid [4-(2-amino-1-aminomethyl-ethyl)-2-cyclohex-1-enyl-phenyl]-amide | HCID 59771233 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 178504234 | HCID 178504234 | 39% |
Reaction Steps
A solution of 4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid[4-(2-amino-1-aminomethyl-ethyl)-2-cyclohex-1-enyl-phenyl]-amide (as prepared in Example 12, step (d), 250 mg, 0.506 mmol) and N-(bis-methylsulfanyl-methylene)-methanesulfonamide (Australian Journal of Chemistry, 46(6), 873, (1993), 100 mg, 0.506 mmol) in 1,2-dichloroethane (20 mL) was heated at reflux for 4 h. The reaction mixture was concentrated, and the residue was purified on silica (20-100% EtOAc-hexane) to obtain the title compound (117 mg, 39%): Mass spectrum, (ESI, m/z): Calcd. for C28H39N7O4SSi, 598.2 (M+H), found 598.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481564B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-bfec5f1283a14a23b86c5e652061da43 |
| Source note | uspto-grants-2013_07 |