Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | 1-Pentanol | HCID 6276 | — |
| Reactant | Thiophene-3,4-diamine | HCID 643216 | — |
| Product | HCID 54035172 | HCID 54035172 | — |
Reaction Steps
To the 3,4-diaminothiophene obtained in Production Example 1 were added 1.1 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 1H-thieno[3,4-d]imidazol-2(3H)-one was obtained. The yield based on 3,4-diaminothiophene was 55%.
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-b46ba77f667f4656819dc998cf0a4a15 |
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| Source note | uspto-grants-2013_08 |
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