Basic information Uses Safety Supplier Related

1-BOC-4-SPIRO-[3-(2-PYRROLIDINONE)] PIPERIDINE

Basic information Uses Safety Supplier Related

1-BOC-4-SPIRO-[3-(2-PYRROLIDINONE)] PIPERIDINE Basic information

Product Name:
1-BOC-4-SPIRO-[3-(2-PYRROLIDINONE)] PIPERIDINE
Synonyms:
  • 1-BOC-4-SPIRO-[3-(2-PYRROLIDINONE)] PIPERIDINE
  • TERT-BUTYL 1-OXO-2,8-DIAZASPIRO[4.5]DECANE-8-CARBOXYLATE
  • 2,8-Diazaspiro[4.5]decane-8-carboxylicacid,1-oxo-,1,1-dimethylethylester
  • 1-Oxo-2,8-diazaspiro[4.5]decane-8-carboxylic acid 1,1-dimethylethyl ester
  • 1-Oxo-2,8-diazaspiro[4.5]decane-8-carboxylic acid tert-butyl ester
  • 1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate
  • 8-Boc-1-oxo-2,8-diazaspiro[4.5]decane
  • tert-butyl 1-oxo-2,8-diazaspiro[4.5]decane-8-carbo
CAS:
268550-48-7
MF:
C13H22N2O3
MW:
254.33
Mol File:
268550-48-7.mol
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1-BOC-4-SPIRO-[3-(2-PYRROLIDINONE)] PIPERIDINE Chemical Properties

Boiling point:
424.9±38.0 °C(Predicted)
Density 
1.15
storage temp. 
2-8°C
pka
16.00±0.20(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C13H22N2O3/c1-12(2,3)18-11(17)15-8-5-13(6-9-15)4-7-14-10(13)16/h4-9H2,1-3H3,(H,14,16)
InChIKey
ADPIEGXXCABJCH-UHFFFAOYSA-N
SMILES
C1(=O)C2(CCN(C(OC(C)(C)C)=O)CC2)CCN1
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Safety Information

HazardClass 
IRRITANT
HS Code 
2932990090
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1-BOC-4-SPIRO-[3-(2-PYRROLIDINONE)] PIPERIDINE Usage And Synthesis

Uses

1-O-2,8-diazaspiro[4.5]decane-8-carboxylic acid tert-butyl ester is a carboxylic acid ester derivative that can be used as a pharmaceutical intermediate in pharmaceutical experimental research and synthesis.

Synthesis

495414-81-8

268550-48-7

B) Synthesis of tert-butyl 1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate 4-(Cyanomethyl)-1,4-piperidinedicarboxylic acid-1-(1,1-dimethylethyl)4-ethyl ester (2.5 g) was dissolved in methanol (50 mL), and cobalt(II) chloride hexahydrate (1.0 g) and sodium borohydride (1.6 g) were added sequentially under ice bath cooling. The reaction mixture was stirred by keeping the ice bath cool for 2 h. Subsequently, the ice bath was removed and stirring was continued for 2 h at room temperature. The reaction system was then warmed to 60°C for 1 hour. After completion of the reaction, 28% ammonia solution was added to the system and the resulting precipitate was removed by filtration. The filtrate was extracted with ethyl acetate, the organic layers were combined and dried over anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure and the resulting crude product was purified by silica gel column chromatography (eluent: ethyl acetate) to afford the target compound tert-butyl 1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate (1.1 g). The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 1.25-1.35 (2H, m), 1.40 (9H, s), 1.45-1.58 (2H, m), 1.90-1.98 (2H, m), 2.90 (2H, brs), 3.16 (2H, t, J=7.2Hz), 3.76-3.86 ( 2H, m), 7.56 (1H, brs).

References

[1] Patent: EP2933247, 2015, A1. Location in patent: Paragraph 0334

1-BOC-4-SPIRO-[3-(2-PYRROLIDINONE)] PIPERIDINESupplier

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