Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | N-tert-butyl-3-oxobutanamide | HCID 257712 | — |
| Product | HCID 19864533 | HCID 19864533 | — |
Reaction Steps
N-t-butyl-3-ketobutanamide (0.29 g) was dissolved in saturated ethanolic ammonia (15 ml) and stirred overnight at room temperature. The solution was evaporated to yield N-t-butyl-3-aminocrotonamide which was used directly. The crude residue was dissolved in ethanol (8 ml), 2-chlorobenzaldehyde (0.28 g) and ethyl 4-[2-(2-methylbenzimidazol-1-yl)ethoxy]-3-ketobutanoate (0.61 g) were added. The mixture was heated at reflux overnight, cooled and the solvent removed under reduced pressure. The residue was chromatographed on silica eluting with 4% diethylamine in ethyl acetate. The fractions containing the product were combined and evaporated. The residue was re-chromatographed on silica eluting with 5% methanol in ethyl acetate. The fractions containing the product were combined and evaporated to yield the title compound (0.17 g, 15%). m.p. 157°-161° C. Found: C, 65.66; H, 6.68; N, 9.74. C31H37C1N4O4 requires C, 65.89; H, 6.60; N, 9.91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801598 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-a3ed0705cf354752aa7c6afb4ede0d38 |
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| Source note | uspto-grants-1989_01 |
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