HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → 5-Cyano-7-(4-methanesulphonylmethylphenyl)-1-phenylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole | HCID 67485006 | — |
| Reactant | 5-Cyano-7-(3-methanesulphonylmethylphenyl)-1-phenylbenzimidazole | HCID 67485556 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Cyano-7-(4-methanesulphonylmethylphenyl)-1-phenylbenzimidazole | HCID 67484990 | — |
Reaction Steps
5-Cyano-7-(4-methanesulphonylmethylphenyl)-1-phenylbenzimidazole was prepared from 5-cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole (500 mg, 1.54 mmol), diisopropylethylamine (0.82 ml, 4.62 mmol) and methanesulphonyl chloride (0.13 ml, 1.69 mmol) in dichloromethane (10 ml) using the method described for 5-cyano-7-(3-methanesulphonylmethylphenyl)-1-phenylbenzimidazole. The crude solution (approximately 0.14 M of product) was used directly in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700638B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-144dffb51cf049ce8c0b03d0764b78d2 |
| Source note | uspto-grants-2010_04 |