HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 12042347, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 949881 | HCID 949881 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12042347 | HCID 12042347 | 62.3% |
Reaction Steps
1-(2-Chlorobenzyl)-2-n-propylbenzimidazole (150 mg) and triethylamine (61 mg) are dissolved in methylene chloride (3 ml). Methanesulfonyl chloride (70 mg) is added to the mixture solution at room temperature, stirred for 1 hour, and then washed with diluted hydrochloric acid. After it is washed with water, it is dried and the solvent is removed through evaporation under reduced pressure. The solid residue is filtered using ether, and 1-(2-chlorobenzyl)-6-mesylamino-2-n-propylbenzimidazole (124 mg) is obtained. 1H-NMR, (CDCl3—CD3OD, δ): 0.94 (3H, t, J=7.5 Hz), 1.76 (2H, m), 2.71 (2H, t, J=7.5 Hz), 2.81 (3H, s), 5.36 (2H, s), 6.40 (1H, d, J=7.5 Hz), 6.98-7.22 (4H,m), 7.40 (1H, d, J=7.5 Hz), 7.59 (1H, d, J=7.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06369092B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-8ee6abf2823f4cc29e5f8f33781687f0 |
| Source note | uspto-grants-2002_04 |