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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 59291346HCID 59291346—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product5,6-Dihydro-2-phenyl-4H-cyclopenta[b]thiophen-3-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367696B2
Source datasetuspto-grants-2013_02
ORD IDord-b7991e372bb94dcc8812754e169cc886
Source noteuspto-grants-2013_02