Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | 1-Pentanol | HCID 6276 | — |
| Reactant | HCID 58399742 | HCID 58399742 | — |
| Product | HCID 46899385 | HCID 46899385 | — |
Reaction Steps
To the resulting 2-[4-(3,4-diaminothien-2-yl)phenyl]thiophene-3,4-diamine were added 2.2 equivalents of urea and amyl alcohol in an amount equivalent to 10 ml/mmol, and under argon gas atmosphere, a reaction was advanced by refluxing at 130° C. for 5 hours, then amyl alcohol was distilled off and the residue was purified by silica gel column chromatography using an ethyl acetate/hexane solvent, so that 4-[4-(2,3-dihydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl)phenyl]-2,3-dihydro-1H-thieno[3,4-d]imidazol-2-one was obtained. The yield based on 2-[4-(3,4-diaminothien-2-yl)phenyl]thiophene-3,4-diamine was 60%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519150B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-8f634269bcc947de81b38aa39c6831bc |
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| Source note | uspto-grants-2013_08 |
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