Identification | Back Directory | [Name]
1,2-DIHYDRO-2-OXO-SPIRO[3H-INDOLE-3,4'-PIPERIDINE]-1'-CARBOXYLIC ACID 1,1-DIMETHYLETHYL ESTER | [CAS]
252882-60-3 | [Synonyms]
-piperidine 1’-Boc-spiro[indoline-3,4’-piperidin]-2-one -Boc-1,2-dihydro-2-oxo-spiro[3h-indole-3,4&rsquo Spiro[indole-3,4'-piperidin]-2(1H)-one,N1'-BOCprotected 1'-BOC-1,2-DIHYDRO-2-OXO-SPIRO[3H-INDOLE-3,4'-PIPERIDINE] tert-butyl 2-oxospiro[indoline-3.4-piperidine]-1-carboxylate tert-butyl 2-oxospiro[1H-indole-3,4'-piperidine]-1'-carboxylate tert-butyl 2-oxo-1,2-dihydrospiro[indole-3,4'-
piperidine]-1'-carboxylate tert-Butyl 2-oxo-1,2-dihydro-1'H-spiro[indole-3,4'-piperidine]-1'-carboxylate 1,1-DiMethylethyl 1,2-dihydro-2-oxospiro[3H-indole-3,4'-piperidine]-1'-carboxylate 1,1-DiMethylethyl 2-oxo-1,2-dihydro-1'H-spiro[indole-3,4'-piperidine]-1'-carboxylate 1,2-DIHYDRO-2-OXO-SPIRO[3H-INDOLE-3,4'-PIPERIDINE]-1'-CARBOXYLIC ACID 1,1-DIMETHYLETHYL ESTER Spiro[3H-indole-3,4'-piperidine]-1'-carboxylic acid, 1,2-dihydro-2-oxo-, 1,1-diMethylethyl ester 1,2-Dihydro-2-oxo-spiro[3h-indole-3,4'-piperidine]-1'-carboxylic acid 1,1-dimethylethyl ester 1,1-Dimethylethyl1,2-dihydro-2-oxospiro[3H-indole-3,4'-piperidine]-1'-carboxylate/tert-butyl 2-oxospiro[indoline-3,4'-piperidine]-1'-carboxylate | [Molecular Formula]
C17H22N2O3 | [MDL Number]
MFCD10566051 | [MOL File]
252882-60-3.mol | [Molecular Weight]
302.37 |
Chemical Properties | Back Directory | [Boiling point ]
475.6±45.0 °C(Predicted) | [density ]
1.22±0.1 g/cm3 (20 ºC 760 Torr) | [storage temp. ]
Sealed in dry,2-8°C | [form ]
powder | [pka]
13.83±0.20(Predicted) | [color ]
Yellow |
Hazard Information | Back Directory | [Synthesis]
Spiro[indoline-3,4'-piperidin]-2-one (2.73 g, 11.42 mmol) and di-tert-butyl dicarbonate (2.74 g, 12.57 mmol) were used as the raw materials. Spiro[indoline-3,4'-piperidin]-2-one was dissolved in tetrahydrofuran (100 mL), and then di-tert-butyl dicarbonate and triethylamine (2.38 mL, 17.135 mmol) were added in turn at room temperature. 17.135 mmol). The reaction mixture was stirred at room temperature for 4 hours. Upon completion of the reaction, the solvent was removed by evaporation under reduced pressure and the residue was treated with a mixture of water and dichloromethane. The aqueous layer was extracted three times with dichloromethane, the organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to give tert-butyl 2-oxospiro[dihydroindole-3,4'-piperidine]-1'-carboxylate (4.02 g, quantitative yield) as a white foam. The product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 1.44 (s, 9H), 1.56-1.73 (m, 4H), 3.55-3.79 (m, 4H), 6.86 (dd, J = 7.70, 0.40 Hz, 1H), 6.95 (td, J = 7.59, 1.10 Hz, 1H), 7.19 (td , J = 7.70, 1.10 Hz, 1H), 7.43 (dd, J = 6.80, 0.70 Hz, 1H), 10.41 (br.s., 1H); m/z = 303.05 (M + H). | [References]
[1] Patent: WO2014/60411, 2014, A1. Location in patent: Page/Page column 36; 37 |
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