HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383913Generated: October 28, 2026
Water → 5,6-Dihydro-2-phenyl-4H-cyclopenta[b]thiophen-3-amine
https://huagongshe.com/reaction/383913
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 59291346 | HCID 59291346 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5,6-Dihydro-2-phenyl-4H-cyclopenta[b]thiophen-3-amine | HCID 59291375 | — |
Reaction Steps
To a solution of 2-phenyl-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylic acid and TEA in toluene was added a solution of DPPA in toluene, followed by stirring at room temperature for 40 minutes, and then stirring at 90° C. for 60 minutes. Furthermore, a solution of (3R)-quinuclidinole in DMF was added thereto, followed by heating under reflux for 15 hours. To the reaction liquid was added water, followed by extraction with EtOAc. The organic layer was washed with water and brine in this order, dried over MgSO4, and then concentrated under reduced pressure. The oily substance obtained was purified by medium-pressure preparative liquid chromatography (silica gel, YAMAZEN YFLC WPrep2XY, hexane:EtOAc) to obtain 2-phenyl-5,6-dihydro-4H-cyclopenta[b]thiophene-3-amine as a pale brown oil, but not a desired (3R)-1-azabicyclo[2.2.2]oct-3-yl(2-phenyl-5,6-dihydro-4H-cyclopenta[b]thien-3-yl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367696B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-b7991e372bb94dcc8812754e169cc886 |
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| Source note | uspto-grants-2013_02 |
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