SPIRO[INDOLINE-3,4'-PIPERIDIN]-2-ONE HYDROCHLORIDE
SPIRO[INDOLINE-3,4'-PIPERIDIN]-2-ONE HYDROCHLORIDE Basic information
- Product Name:
- SPIRO[INDOLINE-3,4'-PIPERIDIN]-2-ONE HYDROCHLORIDE
- Synonyms:
-
- Spiro[3H-indole-3,4'-piperidin]-2(1H)-one, hydrochloride (1:1)
- Spiro[3H-indole-3,4'-piperidin]-2(1H)-one, hydrochloride
- 1,2-Dihydro-2-oxo-spiro[3H-indole-3,4'-piperidine] hydrochloride
- 1,2-Dihydrospiro[indole-3,4'-piperidine]-2-one hydrochloride
- Spiro[indoline-3,4'-piperidin]-2-one, HCl
- spiro[1H-indole-3,4'-piperidine]-2-one,hydrochloride
- Spiro[indoline-3,4'-piperidin]-2-one hydrochloride
- Spiro[3H-indole-3,4′-piperidin]-2(1H)-one Hydrochloride, CAS 356072-46-3
- CAS:
- 356072-46-3
- MF:
- C12H15ClN2O
- MW:
- 238.7133
- Mol File:
- 356072-46-3.mol
SPIRO[INDOLINE-3,4'-PIPERIDIN]-2-ONE HYDROCHLORIDE Chemical Properties
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- White to off-white Solid
SPIRO[INDOLINE-3,4'-PIPERIDIN]-2-ONE HYDROCHLORIDE Usage And Synthesis
Uses
Spiro[3H-indole-3,4''-piperidin]-2(1H)-one Hydrochloride, can be used as high-affinity, selective σ ligands.
Synthesis
356072-45-2
356072-46-3
1'-(Benzyloxycarbonyl)spiro[3H-indole-3,4'-piperidin]-2(1H)-one (74.6 mg) was used as a raw material and dissolved in methanol (1.5 mL). 10% palladium/carbon catalyst (14 mg) was added and the reaction was stirred at room temperature under hydrogen atmosphere for 4 hours. Upon completion of the reaction, the insoluble material was removed by filtration. To the filtrate, 1N aqueous hydrochloric acid (0.33 mL) was added, followed by evaporation of the solvent under reduced pressure to afford spiro[indoline-3,4-piperidin]-2-one hydrochloride (51.7 mg) in 98% yield. The product was characterized by 1H-NMR (D2O): δ 2.11 (4H, m), 3.48 (2H, m), 3.72 (2H, m), 7.07 (1H, d, J = 8 Hz), 7.18 (1H, t, J = 8 Hz), 7.35 (1H, t, J = 8 Hz), 7.45 (1H, d, J = 8 Hz). Mass spectrometry (TSP) analysis showed: m/z 203 (MH+).
References
[1] Patent: US2003/171370, 2003, A1
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