Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 19911564 | HCID 19911564 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19911521 | HCID 19911521 | 79.2% |
Reaction Steps
A mixture of 5.3 parts of chloroacetonitrile, 14.4 parts of 3-(2-ethoxyethyl)-2-(1-piperazinylmethyl)-3H-imidazo[4,5-b]pyridine, 7.4 parts of sodium carbonate and 288 parts of N,N-dimethylformamide was stirred overnight at room temperature. The reaction mixture was stirred into water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was stirred in 2,2'-oxybispropane. The product was filtered off and dried, yielding 13 parts (79.2%) of 4-[[3-(2-ethoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl]-1-piperazineacetonitrile; mp. 80.7° C. (compound 75).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04946843 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-2321dea6e04e4668b3065e9a821f313c |
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| Source note | uspto-grants-1990_08 |
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