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1095708-32-9

1095708-32-9 Structure

1095708-32-9 Structure
IdentificationBack Directory
[Name]

tert-Butyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin -2-yl]carbamate
[CAS]

1095708-32-9
[Synonyms]

Boc-2-AMinopyridine-4-boronic acid pinacol ester
2-(tert-ButoxycarbonylaMino)pyridine-4-boronic acid pinacol ester
(2-((TERT-BUTOXYCARBONYL)AMINO)PYRIDIN-4-YL)BORONIC ACID PINACOL ESTER
tert-butyl N-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate
N-tert-butyl-N-[3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbaMate
tert-Butyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin -2-yl]carbamate
tert-butyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate
tert-butyl (4-(hydroxy((3-hydroxy-2,3-dimethylbutan-2-yl)oxy)boranyl)pyridin-2-yl)carbamate
[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridin-2-yl]-carbamic acid tert-butyl ester 97%
Carbamic acid, N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinyl]-, 1,1-dimethylethyl ester
[Molecular Formula]

C16H25BN2O4
[MDL Number]

MFCD12032217
[MOL File]

1095708-32-9.mol
[Molecular Weight]

320.19
Chemical PropertiesBack Directory
[Boiling point ]

400.7±30.0 °C(Predicted)
[density ]

1.10
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[pka]

12.66±0.70(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Spectrum DetailBack Directory
[Spectrum Detail]

tert-Butyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin -2-yl]carbamate (1095708-32-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

TERT-BUTYL 4-BROMOPYRIDIN-2-YLCARBAMATE

207799-10-8

Bis(pinacolato)diboron

73183-34-3

tert-Butyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin
-2-yl]carbamate

1095708-32-9

A reaction mixture was prepared in dimethyl sulfoxide (8 mL) with 2-Boc amine-4-bromopyridine (0.494 g, 1.81 mmol), pinacol ester of bisboronic acid (1.4 g, 5.51 mmol) and potassium acetate (0.535 g, 5.45 mmol). The mixture was purged with nitrogen for 10 min to deoxygenate. Subsequently, [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloride (0.150 g, 0.184 mmol) was added and again purged with nitrogen for 5 min. Under nitrogen protection, the reaction mixture was heated to 85 °C and stirred for 1 hour. Upon completion of the reaction, the mixture was diluted with ethyl acetate (15 mL) and washed with 0.2 M aqueous hydrochloric acid (10 mL). Note that some of the product may be present in the aqueous layer. Carefully adjust the pH of the aqueous layer to about 6 with saturated aqueous sodium carbonate, and then extract the product from the aqueous layer with ethyl acetate (10 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated in vacuum to afford 2-(Boc-amino)pyridine-4-boronic acid pinacol ester as a white solid (0.44 g, 76% yield). The product was characterized by 1H NMR (DMSO-d6) and LCMS: 1H NMR (DMSO-d6) δ 1.29 (s, 12H), 1.45 (s, 9H), 7.15-7.17 (d, 1H), 8.07 (s, 1H), 8.24-8.25 (d, 1H), 9.77 (s, 1H); LCMS Rt = 0.68 min, MS m/z 183.1 [M+H]+.

[References]

[1] Journal of Medicinal Chemistry, 2017, vol. 60, # 13, p. 5613 - 5637
[2] Patent: WO2012/4714, 2012, A2. Location in patent: Page/Page column 62
[3] Patent: US2014/194443, 2014, A1. Location in patent: Paragraph 0543-0545
[4] Patent: WO2014/108337, 2014, A1. Location in patent: Page/Page column 69; 70
[5] Patent: US2010/179154, 2010, A1. Location in patent: Page/Page column 29
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