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392331-66-7

392331-66-7 Structure

392331-66-7 Structure
IdentificationBack Directory
[Name]

tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate
[CAS]

392331-66-7
[Synonyms]

1-Boc-4-(Aminomethyl)
1-Boc-4-aMinoMethyl-4-hyd...
4-Aminomethyl-1-Boc-piperidin-4-ol
4-AMinoMethyl-1-Boc-4-hydroxypiperidine, 97%
tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate
1-Piperidinecarboxylic acid, 4-(aminomethyl)-4-hydroxy-, 1,1-dimethylethyl ester
[Molecular Formula]

C11H22N2O3
[MDL Number]

MFCD11579803
[MOL File]

392331-66-7.mol
[Molecular Weight]

230.306
Chemical PropertiesBack Directory
[Boiling point ]

341.0±27.0 °C(Predicted)
[density ]

1.124
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

Solid
[pka]

12.48±0.20(Predicted)
[color ]

Off-white
[Water Solubility ]

Slightly soluble in water.
[Sensitive ]

Air Sensitive
[InChI]

InChI=1S/C11H22N2O3/c1-10(2,3)16-9(14)13-6-4-11(15,8-12)5-7-13/h15H,4-8,12H2,1-3H3
[InChIKey]

XYWCDAFPRBDRER-UHFFFAOYSA-N
[SMILES]

N1(C(OC(C)(C)C)=O)CCC(CN)(O)CC1
[CAS DataBase Reference]

392331-66-7
Safety DataBack Directory
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

4-Aminomethyl-1-Boc-4-hydroxypiperidine can be used in agrochemical, pharmaceutical and dyestuff.
[Synthesis]

1-OXA-6-AZASPIRO[2.5]OCTANE-6-CARBOXYLIC ACID, 1,1-DIMETHYLETHYL ESTER

147804-30-6

tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate

392331-66-7

General procedure for the synthesis of tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate from tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate: In a 100 mL sealed tube, a magnetic stirring bar, tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate (300 mg, 1.28 mmol) and 7 M ammonium hydroxide in a methanol solution (20 mL). The reaction mixture was placed in an oil bath at 80°C and stirred for 16 hours. After completion of the reaction, the mixture was cooled to room temperature. The solvent was removed by concentration under reduced pressure to afford the crude product tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate (350 mg, >95% yield), which could be used in the subsequent reaction without further purification.LCMS (ESI) m/z 231 [M + H]+.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 24, p. 7458 - 7461
[2] Patent: US2016/185786, 2016, A1. Location in patent: Paragraph 0679
[3] Patent: WO2015/92804, 2015, A1. Location in patent: Page/Page column 21
[4] European Journal of Medicinal Chemistry, 2015, vol. 103, p. 289 - 301
[5] Patent: WO2014/147636, 2014, A1. Location in patent: Page/Page column 35; 36
Spectrum DetailBack Directory
[Spectrum Detail]

tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate(392331-66-7)1HNMR
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