1-Oxa-3,8-diazaspiro(4.5)decan 2-one
- Product Name
- 1-Oxa-3,8-diazaspiro(4.5)decan 2-one
- CAS No.
- 5052-95-9
- Chemical Name
- 1-Oxa-3,8-diazaspiro(4.5)decan 2-one
- Synonyms
- 1-Oxa-3,8-diazaspiro(4.5)decan 2-one;1-oxy-3,8-diazaspiro[4.5]decylalkane-2-one;1-oxa-3,8-diazaspiro[4.5]decan-2-one - [X23979];1-oxa-3,8-diazaspiro[4.5]decan-2-one(SALTDATA: HCl)
- CBNumber
- CB91357458
- Molecular Formula
- C7H12N2O2
- Formula Weight
- 156.18
- MOL File
- 5052-95-9.mol
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- CHM0304716
- Product name
- 1-OXA-3,8-DIAZASPIRO[4.5]DECAN-2-ONE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $495.07
- Updated
- 2021/12/16
- Product number
- 6962AB
- Product name
- 1-Oxa-3,8-diazaspiro[4.5]decan-2-one
- Packaging
- 1g
- Price
- $821.6
- Updated
- 2021/12/16
- Product number
- SC-94986
- Product name
- 1-Oxa-3,8-diazaspiro[4.5]decan-2-one
- Purity
- 95
- Packaging
- 5g
- Price
- $1617
- Updated
- 2021/12/16
- Product number
- CM139344
- Product name
- 1-Oxa-3,8-diaza-spiro[4.5]decan-2-one
- Purity
- 95%
- Packaging
- 1g
- Price
- $505
- Updated
- 2021/12/16
- Product number
- CD11114450
- Product name
- 1-Oxa-3,8-diazaspiro[4.5]decan-2-one
- Purity
- 95+%
- Packaging
- 1g
- Price
- $540
- Updated
- 2021/12/16
1-Oxa-3,8-diazaspiro(4.5)decan 2-one Chemical Properties,Usage,Production
Synthesis
5053-14-5
5052-95-9
General procedure for the synthesis of 1-oxo-3,8-diazaspiro[4,5]decan-2-one from 8-benzyl-1-oxo-3,8-diazaspiro[4,5]decan-2-one: 8-benzyl-1-oxo-3,8-diazaspiro[4,5]decan-2-one (170 mg, 0.69 mmol) was dissolved in methanol (20 mL), ammonium formate (261 mg) and 10% Pd/C (89 mg). The reaction mixture was stirred and refluxed for 1.5 h at room temperature. After completion of the reaction, the mixture was filtered through a diatomaceous earth pad and the solvent was removed under vacuum. The residue was dissolved in methanol and the solution was allowed to pass through a SCX column pre-washed with methanol and eluted with a methanol solution of 2N ammonia to afford 1-oxo-3,8-diazaspiro[4,5]decan-2-one (80 mg, 74% yield). Mass spectrum (electrospray ionization) (m/z): 157.0 [M+H]+.
References
[1] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 4, p. 340 - 345
[2] Patent: WO2016/42452, 2016, A1. Location in patent: Page/Page column 202
[3] Chimica Therapeutica, 1969, vol. 4, p. 185 - 194
[4] Journal of Medicinal Chemistry, 1981, vol. 24, # 11, p. 1320 - 1328
[5] Journal of Medicinal Chemistry, 2016, vol. 59, # 3, p. 1078 - 1101
1-Oxa-3,8-diazaspiro(4.5)decan 2-one Preparation Products And Raw materials
Raw materials
Preparation Products
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