HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 5-(2-Methylsulphonylaminomethyl-prop-2-yl)-2-(4-pyridinyl)-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 5-(2-Aminomethylprop-2-yl)-2-(4-pyridinyl)-benzimidazole | HCID 14153027 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(2-Methylsulphonylaminomethyl-prop-2-yl)-2-(4-pyridinyl)-benzimidazole | HCID 14153045 | — |
Reaction Steps
To 2.0 g. of the 5-(2-aminomethylprop-2-yl)-2-(4-pyridinyl)-benzimidazole (prepared in Example 1) and 830 mg. triethylamine in 50 ml. dry dichloromethane are added dropwise, while cooling with ice water, 953 mg. mesyl chloride. The reaction mixture is stirred for 10 minutes and then 20 ml. water are added thereto. After filtering off with suction, washing with water and dichloromethane and recrystallising from water/ethanol (2:1 v/v), there are obtained 2.0 g. (85% of theory) of the title compound as a hydrate in the form of yellowish crystals which sinter above 130° C., again crystalline above 150° C. and then melt at 215°-216° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04882342 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-3f30f5acf22b419493bb21763ca2fb6e |
| Source note | uspto-grants-1989_11 |