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130309-46-5

130309-46-5 Structure

130309-46-5 Structure
IdentificationBack Directory
[Name]

4-(BOC-AMINO)CYCLOHEXANECARBOXYLIC ACID
[CAS]

130309-46-5
[Synonyms]

4-(BOC-AMINO)CYCLOHEXANECARBOXYLIC ACID
4-N-BOC-AMINOCYCLOHEXANE CARBOXYLIC ACID
4-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID
4-Aminocyclohexane-1-carboxylic acid, N-BOC protected
1-(t-Butyloxycarbonylamino)cyclohexyl-4-carboxylic acid
4-Aminocyclohexane-1-carboxylic acid, N-BOC protected 98%
4-[(tert-Butoxycarbonyl)amino]cyclohexane-1-carboxylic acid
4-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclohexanecarboxylic acid
Cyclohexanecarboxylicacid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-
4-[(2-methylpropan-2-yl)oxycarbonylamino]cyclohexane-1-carboxylic acid
4-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-1-cyclohexanecarboxylic acid
4-(tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid (cis- and trans- mixture)
4-(tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid (cis- and trans- mixture)>
4-(tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid (cis- and trans- mixture)
[Molecular Formula]

C12H21NO4
[MDL Number]

MFCD03453262
[MOL File]

130309-46-5.mol
[Molecular Weight]

243.3
Chemical PropertiesBack Directory
[Boiling point ]

396.7±31.0 °C(Predicted)
[density ]

1.12
[storage temp. ]

2-8°C
[solubility ]

Soluble in methanol and tetrahydrofuran(THF).
[form ]

powder to crystal
[pka]

4.76±0.10(Predicted)
[color ]

White to Almost white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[WGK Germany ]

3
[HS Code ]

2922498590
Hazard InformationBack Directory
[Uses]

4-(Boc-amino)cyclohexanecarboxylic acid is used as pharmaceutical intermediate.
[Synthesis]

Di-tert-butyl dicarbonate

24424-99-5

4-AMINOCYCLOHEXANECARBOXYLIC ACID

1776-53-0

CIS-4-(BOC-AMINO)CYCLOHEXANECARBOXYLIC ACID

53292-90-3

To a stirred solution of trans-4-aminocyclohexanecarboxylic acid (1 g, 6.98 mmol) in tert-butanol (10 mL) and NaOH (0.307 g, 7.68 mmol) in water (10 mL) was slowly added di-tert-butyl dicarbonate (1.7 g, 7.68 mmol) at 0 °C. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, hexane (50 mL) was added to the mixture and the pH was adjusted to about 6 with 6 N HCl. Subsequently, the mixture was extracted with ethyl acetate (3 x 50 mL) and the organic phases were combined and washed with saturated brine solution (25 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the white powdery product cis-4-((tert-butoxycarbonyl)amino)cyclohexanecarboxylic acid (1.4 g, 82.8% yield). Mass spectrum (ES-) m/z 242 [M-H]-.

[References]

[1] Patent: US2017/348315, 2017, A1. Location in patent: Paragraph 0400
[2] Patent: WO2010/45987, 2010, A1. Location in patent: Page/Page column 43-44
[3] European Journal of Medicinal Chemistry, 2001, vol. 36, # 3, p. 265 - 286
[4] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 2, p. 89 - 93
Spectrum DetailBack Directory
[Spectrum Detail]

4-(BOC-AMINO)CYCLOHEXANECARBOXYLIC ACID(130309-46-5)1HNMR
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