Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | HCID 178488841 | HCID 178488841 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 54192258 | HCID 54192258 | — |
Reaction Steps
1.9 g. 4-(2-Aminomethylpropan-2-yl)-2-(4-methoxyphenyl)-benzimidazole (obtained in Example 6) in 200 ml. dichloromethane are reacted with 2.5 ml. triethylamine and 0.82 g. isobutyric acid chloride at ambient temperature. After 10 hours, the solvent is removed in a vacuum and the residue is digested with water and 2N aqueous ammonia solution. The reaction mixture is extracted 4 times with dichloromethane and the organic phase is dried over anhydrous sodium sulphate, filtered and evaporated. Ethyl acetate is added thereto, a part thereof is distilled off with the dichloromethane and left to crystallise and the product is filtered with suction. The product is recrystallised from ethyl acetate to give 0.6 g. of the title compound; m.p. 218°-220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04882342 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-40bc2e5cef4a4e9e8b5f98d74ea9998f |
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| Source note | uspto-grants-1989_11 |
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