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169280-83-5

169280-83-5 Structure

169280-83-5 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL [5-(HYDROXYMETHYL)PYRIDIN-2-YL)CARBAMATE
[CAS]

169280-83-5
[Synonyms]

tert-butyl 5-(hydroxyMeth...
2-(Boc-amino)-5-pyridinemethanol
2-(Boc-amino)-5-pyridinemethanol ,97%
N-Boc-5-(hydroxymethyl)-2-pyridineamine
tert-butyl N-[5-(hydroxymethyl)pyridin-2-yl]carbamate
2-(tert-Butoxycarbonylamino)-5-(hydroxymethyl)pyridine
6-(N-tert-Butoxycarbonylamino)-3-hydroxymethylpyridine
N-[5-(hydroxymethyl)-2-pyridinyl]carbamic acid tert-butyl ester
CarbaMic acid, N-[5-(hydroxyMethyl)-2-pyridinyl]-, 1,1-diMethylethyl ester
[EINECS(EC#)]

-0
[Molecular Formula]

C11H16N2O3
[MDL Number]

MFCD07186264
[MOL File]

169280-83-5.mol
[Molecular Weight]

224.26
Chemical PropertiesBack Directory
[Boiling point ]

332.8±32.0 °C(Predicted)
[density ]

1.209
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

12.35±0.70(Predicted)
[Appearance]

White to off-white Solid
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
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37
[HS Code ]

29309090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methanol-->Tetrahydrofuran-->Thionyl chloride-->Acetic anhydride-->Lithium Aluminum Hydride-->Acetonitrile-->Di-tert-butyl dicarbonate-->6-Aminonicotinic acid-->3-Pyridinecarboxylic acid, 6-[[(1,1-diMethylethoxy)carbonyl]aMino]-, ethyl ester-->Ethyl 6-(bis-tert-butoxycarbonyl)aminonicotinat
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Synthesis]

3-Pyridinecarboxylic acid, 6-[[(1,1-diMethylethoxy)carbonyl]aMino]-, ethyl ester

169280-82-4

TERT-BUTYL [5-(HYDROXYMETHYL)PYRIDIN-2-YL)CARBAMATE

169280-83-5

To a stirred solution of ethyl 6-(tert-butoxycarbonylamino)nicotinate (100; 10.0 g, 27.3 mmol) in tetrahydrofuran (THF) (40 mL) was slowly added a solution of lithium aluminum hydroxide (LA1H4) (1.92 g, 50.5 mmol) in THF (60 mL) over 30 min, keeping the reaction temperature not below 0 °C. The reaction mixture was continued to be stirred at 0 °C for 6 hours. Upon completion of the reaction, water (1.0 mL) and 10% sodium hydroxide (NaOH) solution (2.0 mL) were carefully added at 0 °C to quench the reaction. The resulting mixture was filtered and the filtrate was dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. The residue was purified by column chromatography (eluent ratio dichloromethane: methanol = 40:1) to afford the target product tert-butyl 5-(hydroxymethyl)pyridin-2-ylcarbamate 101 (4.50 g, 74% yield).

[References]

[1] Patent: WO2010/3048, 2010, A1. Location in patent: Page/Page column 110
[2] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 5, p. 1151 - 1175
[3] Patent: WO2014/52365, 2014, A1. Location in patent: Page/Page column 257-258
[4] Patent: US6046190, 2000, A
[5] Patent: US5968942, 1999, A
Spectrum DetailBack Directory
[Spectrum Detail]

TERT-BUTYL [5-(HYDROXYMETHYL)PYRIDIN-2-YL)CARBAMATE(169280-83-5)1HNMR
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