Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate

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Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate manufacturers

Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate Basic information
Product Name:Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate
Synonyms:Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate;Carbamic acid, N-[(5-bromo-2-pyridinyl)methyl]-, 1,1-dimethylethyl ester;tert-butyl N-[(5-bromo-2-pyridyl)methyl]carbamate
CAS:1188477-11-3
MF:C11H15BrN2O2
MW:287.15
EINECS:
Product Categories:
Mol File:1188477-11-3.mol
Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate Structure
Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate Chemical Properties
Melting point 92-94 °C
Boiling point 372.4±32.0 °C(Predicted)
density 1.367±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka11.14±0.46(Predicted)
AppearanceWhite to light yellow Solid
Safety Information
MSDS Information
Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate Usage And Synthesis
Synthesis
Di-tert-butyl dicarbonate

24424-99-5

5-Bromo-2-pyridinecarbonitrile

97483-77-7

Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate

1188477-11-3

GENERAL STEPS: To a solution of 5-bromo-2-cyanopyridine (3.0 g, 16.4 mmol) in methanol (60 mL) was sequentially added di-tert-butyl dicarbonate (7.2 g, 32.8 mmol) and nickel chloride hexahydrate (0.33 g, 1.64 mmol). The reaction mixture was cooled to 0 °C, followed by the addition of sodium borohydride (4.3 g, 0.115 mol) in batches over a period of 2 hours. The reaction mixture was continued to be stirred at 15 °C for 1 h, after which it was poured into ice water (200 g) and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by fast column chromatography to afford the target product tert-butyl (5-bromopyridin-2-ylmethyl)carbamate (2.2 g, 47% yield) as a yellow solid. m/z 287,289 ([M+H]+) by LC-MS.

References[1] Patent: WO2016/112088, 2016, A1. Location in patent: Paragraph 0660
[2] Patent: US2013/237502, 2013, A1. Location in patent: Paragraph 0367
[3] Patent: WO2018/42342, 2018, A1. Location in patent: Page/Page column 53
Tert-Butyl5-Bromopyridin-2-yl(methyl)carbamate Preparation Products And Raw materials
Raw materials5-Bromopyridine-2-carbaldehyde-->Di-tert-butyl dicarbonate-->5-Bromo-2-pyridinecarbonitrile-->tert-Butyl carbamate-->Methanol-->Nickel(II) chloride hexahydrate-->Sodium borohydride
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