Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 26804 | HCID 26804 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-((1,1-dimethylethoxy)carbonyl)-beta-alanine | HCID 76809 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70632980 | HCID 70632980 | — |
Reaction Steps
t-Butoxycarbonyl -β-alanine (16.1 g, 0.080 mole) in dimethylformamide (200 ml) was cooled to 0°, and triethylamine (23.8 ml, 0.17 mole) was rapidly added. The solution was kept at -5° to 0° while isobutylchloroformate (11.9 ml, 0.085 mole) was added dropwise. The solution was stirred 10 minutes and then 1-{[5-(4-cyanophenyl)furfurylidene]amino}hydantoin (recrystallized and predried at 100° overnight; 23.5 g, 0.080 mole) was rapidly added. The mixture was maintained at -5° to 0° for 0.5 hr and was then stirred 1 hour without cooling. The mixture was poured into a solution of ice water (1,400 ml) and concentrated hydrochloric acid (25 ml). The resulting solid was collected and air-dried. The product was dissolved in acetonitrile, filtered, and concentrated to a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001222 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-a1d7c8db18c64c5aa546ec0bc26d01a2 |
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| Source note | uspto-grants-1977_01 |
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