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1121057-77-9

1121057-77-9 Structure

1121057-77-9 Structure
IdentificationBack Directory
[Name]

tert-butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydropyridine-1(2H)-carboxylate
[CAS]

1121057-77-9
[Synonyms]

N-boc-3,4-dihydropiperidine-5-boronic acid pinacol ester
tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dih
tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydropyridine-1
(1-(TERT-BUTOXYCARBONYL)-1,4,5,6-TETRAHYDROPYRIDIN-3-YL)BORONIC ACID PINACOL ESTER
tert-butyl 5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4-tetrahydropyridine-1-carboxylate
tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydropyridine-1(2H)-carboxyla
1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C16H28BNO4
[MDL Number]

MFCD18383341
[MOL File]

1121057-77-9.mol
[Molecular Weight]

309.21
Chemical PropertiesBack Directory
[Boiling point ]

339.6±52.0 °C(Predicted)
[density ]

1.05±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[pka]

-0.31±0.40(Predicted)
[Appearance]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332
[Precautionary statements ]

P260-P280-P301+P312
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

tert-butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydropyridine-1(2H)-carboxylate(1121057-77-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

tert-butyl 5-{[(trifluoromethyl)sulfonyl]oxy}-3,4-dihydropyridine-1(2H)-carboxylate(SALTDATA: FREE)

149108-74-7

Bis(pinacolato)diboron

73183-34-3

tert-butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydropyridine-1(2H)-carboxylate

1121057-77-9

Step 4. tert-Butyl 5-(((trifluoromethyl)sulfonyl)oxy)-3,4-dihydropyridine-1(2H)-carboxylate (1.45 g, 4.38 mmol) and pinacol ester of bisboronic acid (1.223 g, 4.81 mmol) were dissolved in dioxane (24 mL). To this solution was added potassium acetate (1.289 g, 13.13 mmol) and PdCl2(dppf)-CH2Cl2 adduct (0.107 g, 0.131 mmol). The reaction mixture was purged for 5 min under nitrogen protection and subsequently heated in an oil bath at 80 °C overnight. After completion of the reaction, the mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by fast chromatography using a 0-30% ethyl acetate/heptane gradient elution to afford the target product tert-butyl 5-boronic acid pinacol esteryl-3,4-dihydropyridine-1(2H)-carboxylate as a highly viscous liquid (1.2 g, 89% yield).LCMS (m/z): 254.1 (MH+ - tBu), retention time 1.21 min.

[References]

[1] Patent: US9242996, 2016, B2. Location in patent: Page/Page column 385; 386; 388; 389
[2] Patent: WO2018/203256, 2018, A1. Location in patent: Page/Page column 36
[3] Patent: US2013/102601, 2013, A1. Location in patent: Paragraph 184
[4] Patent: US2013/102600, 2013, A1. Location in patent: Page/Page column 0169; 0171
[5] Patent: WO2015/48662, 2015, A2. Location in patent: Page/Page column 44-45
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