HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979059Generated: October 29, 2026
HCID 11149822, compound → HCID 18331717, compound
https://huagongshe.com/reaction/1979059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11149822 | HCID 11149822 | — |
| Reactant | HCID 11242609 | HCID 11242609 | — |
| Reactant | HCID 11437086 | HCID 11437086 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18331717 | HCID 18331717 | 70% |
Reaction Steps
2.06 g (7.72 mmol) of the mixture of 3-isopropoxycarbonylamino-{2-(E)-(4-methyl-2-penten-2-yl)}thiophene, 3-isopropoxycarbonylamino-{2-(Z)-(4-methyl-2-penten-2-yl)}thiophene, and 3-isopropoxycarbonylamino-{2-(4-methyl-1-penten-2-yl) }thiophene obtained in Example 13 and 0.41 g of 5% palladium carbon (Degussa chemical catalyst E106R/W) were charged into 20 ml of methanol, and after nitrogen purge, a hydrogenation reaction was conducted at normal pressure under hydrogen atmosphere for 9 hours. After nitrogen purge, the catalyst was filtrated off, and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1) to obtain 1.61 g of the intended compound as a colorless crystal (yield: 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06239282B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-14c1bd2cbd79493699d505f09651e037 |
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| Source note | uspto-grants-2001_05 |
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