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ChemicalBook--->CAS DataBase List--->27514-07-4

27514-07-4

27514-07-4 Structure

27514-07-4 Structure
IdentificationBack Directory
[Name]

7-Azabicyclo[2,2,1]heptane hydrochloride
[CAS]

27514-07-4
[Synonyms]

SW-74
SWF-74
7-AZABICYCLO[2,2,1]HEPTANE HCL
7-AZABICYCLO[2.2.1]HEPTANE HYDROCHLORIDE
7-Azabicyclo[2.2.1]heptane, hydrochloride (1:1)
[Molecular Formula]

C6H12ClN
[MDL Number]

MFCD00154183
[MOL File]

27514-07-4.mol
[Molecular Weight]

133.62
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

White to yellow Solid
[InChI]

InChI=1S/C6H11N.ClH/c1-2-6-4-3-5(1)7-6;/h5-7H,1-4H2;1H
[InChIKey]

JQHCKZLQJDVZPH-UHFFFAOYSA-N
[SMILES]

C12CCC(CC1)N2.Cl
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

36/37/38-22
[Safety Statements ]

26-36/37/39
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

7-Azabicyclo[2,2,1]heptane hydrochloride(27514-07-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

7-Azabicyclo[2.2.1]heptane, 7-[(4-methylphenyl)sulfonyl]-

188624-92-2

7-Azabicyclo[2,2,1]heptane hydrochloride

27514-07-4

The compound (CAS: 188624-92-2, 380 g, 1.51 mol) was dissolved in tetrahydrofuran (THF, 3 L) under nitrogen protection and cooled to 0°C. Lithium aluminum hydride (229.4 g, 6.04 mol) solid pellets were added in batches over a period of 2 hours. The reaction mixture was gradually warmed to room temperature with continuous stirring for 4 days until HPLC analysis showed complete consumption of the feedstock. Upon completion of the reaction, the reaction mixture was diluted with THF (11 L) and re-cooled to 0°C. Under rapid stirring, sodium sulfate decahydrate solid was added slowly over a period of 2 h until gas release ceased. The insoluble material was removed by filtration and the filtrate was acidified with gaseous hydrogen chloride to produce a white precipitate. The precipitate was collected by filtration, washed with THF (2 x 500 mL) and dried to constant weight to give 7-azabicyclo[2,2,1]heptane hydrochloride (M1, batch 1: 86.8 g, 43%; batch 2: 97.3 g, 49%). The filter cake from the first filtration was resuspended in 6 N sodium hydroxide solution (400 mL) and filtered. The filtrate was extracted with ether (4 L) and the organic layer was acidified with gaseous hydrogen chloride, again producing a white precipitate. The precipitate was collected by filtration, washed with ether (2 x 500 mL) and dried in a vacuum oven at 40 °C to constant weight to give finally 7-azabicyclo[2,2,1]heptane hydrochloride (M I.HCl, 105.9 g, 72%).

[References]

[1] Patent: WO2005/79805, 2005, A1. Location in patent: Page/Page column 61
[2] Tetrahedron, 2009, vol. 65, # 29-30, p. 5805 - 5816
[3] Patent: WO2005/80402, 2005, A1. Location in patent: Page/Page column 65
[4] Patent: WO2005/79805, 2005, A1. Location in patent: Page/Page column 61
[5] Organic Letters, 2001, vol. 3, # 9, p. 1371 - 1373
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