Basic information Safety Supplier Related

2-Boc-7-oxo-2-Azaspiro[4.4]nonane

Basic information Safety Supplier Related

2-Boc-7-oxo-2-Azaspiro[4.4]nonane Basic information

Product Name:
2-Boc-7-oxo-2-Azaspiro[4.4]nonane
Synonyms:
  • 2-Boc-7-oxo-2-Azaspiro[4.4]nonane
  • tert-butyl 7-oxo-2-azaspiro[4.4]nonane-2-carboxylate
  • 2-Boc-7-oxo-2-Azaspiro[4.4]nonane - X10653
  • tert-butyl 7-oxo-2-azaspiro[4.4]nonane-2-carboxylate(WX101862)
  • 2-Azaspiro[4.4]nonane-2-carboxylic acid, 7-oxo-, 1,1-dimethylethyl ester
  • 2-Boc-2-azaspiro[4.4]nonan-7-one
CAS:
1319716-42-1
MF:
C13H21NO3
MW:
239.31
Mol File:
1319716-42-1.mol
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2-Boc-7-oxo-2-Azaspiro[4.4]nonane Chemical Properties

Boiling point:
348.6±25.0 °C(Predicted)
Density 
1.12±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
-0.76±0.20(Predicted)
Appearance
White to light yellow Solid
CAS DataBase Reference
1319716-42-1
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2-Boc-7-oxo-2-Azaspiro[4.4]nonane Usage And Synthesis

Uses

tert-Butyl 7-Oxo-2-azaspiro[4.4]nonane-2-carboxylate is a useful reagent for preparing inhibitors of the menin-MLL interaction.

Synthesis

1319716-41-0

1319716-42-1

7-Hydroxy-2-azaspiro[4.4]nonane-2-carboxylic acid tert-butyl ester (2.10 g, 8.70 mmol) was used as starting material and suspended in anhydrous dichloromethane (25 mL). Dess-Martin oxidizer (4.43 g, 10.44 mmol) was added to the suspension at 0 °C and under nitrogen protection. Subsequently, the reaction mixture was warmed to room temperature and stirred overnight. Upon completion of the reaction, the mixture was cooled to 0 °C, diluted by the addition of dichloromethane (50 mL), and then quenched by the addition of saturated aqueous sodium bicarbonate (30 mL) and saturated aqueous sodium thiosulfate (30 mL), in that order. The organic phase was separated and washed again with a mixture of saturated aqueous sodium bicarbonate solution (15 mL) and saturated aqueous sodium thiosulfate solution (15 mL). The aqueous phase was back-extracted with dichloromethane (50 mL × 3). All organic phases were combined, washed with saturated brine (50 mL), dried over anhydrous sodium sulfate, and filtered. The residue was purified by silica gel column chromatography (petroleum ether/ethyl acetate, v/v = 3/1) to afford tert-butyl 7-oxo-2-azaspiro[4.4]nonane-2-carboxylate as a yellow liquid (1.30 g, 62% yield). Mass spectrum (ESI, positive ion mode) m/z: 184.2 [(M-C4H8)+ H]+; 1H NMR (600 MHz, CDCl3) δ (ppm): 3.56-3.36 (m, 2H), 3.36-3.24 (m, 2H), 2.39-2.32 (m, 2H), 2.32-2.19 (m, 2H), 2.04 -1.91 (m, 2H), 1.90-1.82 (m, 2H), 1.47 (s, 9H).

References

[1] Patent: WO2015/94803, 2015, A1. Location in patent: Paragraph 382
[2] Patent: WO2016/190847, 2016, A1. Location in patent: Paragraph 0394
[3] Patent: CN104974163, 2017, B. Location in patent: Paragraph 0725; 0726; 0727; 0728
[4] Patent: CN104672250, 2017, B. Location in patent: Paragraph 0688; 0689; 0690; 0691
[5] Tetrahedron Letters, 2011, vol. 52, # 32, p. 4204 - 4206

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