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ChemicalBook CAS DataBase List tert-Butyl 4-((6-bromopyridin-3-yl)methyl)piperazine-1-carboxylate
1160923-86-3

tert-Butyl 4-((6-bromopyridin-3-yl)methyl)piperazine-1-carboxylate synthesis

1synthesis methods
149806-06-4 Synthesis
2-Bromopyridine-5-carbaldehyde

149806-06-4
445 suppliers
$5.00/1g

57260-71-6 Synthesis
1-BOC-Piperazine

57260-71-6
725 suppliers
$5.00/5g

tert-Butyl 4-((6-bromopyridin-3-yl)methyl)piperazine-1-carboxylate

1160923-86-3
26 suppliers
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Yield:1160923-86-3 78%

Reaction Conditions:

with sodium tris(acetoxy)borohydride;acetic acid in dichloromethane at 15 - 25; for 24 h;

Steps:

t-Butyl 4-((6-bromopyridin-3-yl)methyl)piperazine-l-carboxylate (iii)

A solution of 5-bromopyridine-2-carbaldehyde (i; 71.4 g, 384 mmol, 1 equiv), 1-Boc- piperzine (ii; 72.8 g, 391 mmol, 1.02 equiv), dichloromethane (1.2 L), and acetic acid (2.4 mL) was cooled to 15 °C and sodium triacetoxyborohydride (164.9 g, 777.8 mmol, 2.03 equiv) was added portionwise to the mixture at 25 °C. The resulting solution was stirred for 24 h at room temperature. An additional portion of sodium triacetoxyborohydride (13 g, 61.3 mmol, 0.16 equiv) was added portionwise at 15 °C. The reaction was then quenched with aq 2N NaOH (250 mL) and the resulting solution was stirred for another 0.5 h. The organic layer was washed twice with water, dried and concentrated. The residue was recrystallized with 4:1 petroleum ether/ethyl acetate to yield 107.7 g (78% yield) of iii as a light yellow solid.

References:

WO2019/148161,2019,A1 Location in patent:Page/Page column 22; 23

tert-Butyl 4-((6-bromopyridin-3-yl)methyl)piperazine-1-carboxylate Related Search:

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