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ChemicalBook CAS DataBase List tert-butyl 4-(isoquinolin-5-yl)piperazine-1-carboxylate
444620-69-3

tert-butyl 4-(isoquinolin-5-yl)piperazine-1-carboxylate synthesis

5synthesis methods
24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
835 suppliers
$13.50/25G

209733-17-5 Synthesis
5-(1-piperazinyl)-isoquinoline HCl

209733-17-5
22 suppliers
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tert-butyl 4-(isoquinolin-5-yl)piperazine-1-carboxylate

444620-69-3
22 suppliers
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Yield:444620-69-3 0.86 g

Reaction Conditions:

with sodium hydroxide in 1,4-dioxane;Cooling with ice;

Steps:



To 5-(piperazin-l-yl)isoquinoline, HCl (0.58 g, 2.322 mmol) and NaOH (5.1 1 mL, 5.11 mmol) in dioxane (6 mL), cooled in ice bath, was added BOC2O (0.539 mL, 2.322 mmol) in dioxane (6 mL). The organics were stripped and the reaction was partitioned with H2O (30mL) and EtOAc (100 mL). The organic layer was washed with brine (15 mL) and dried (MgSO4). Collected Boc-protected compound as a yellow oil (0.86 g) which was then hydrogenated at 55 psi with PtO2 in EtOH. The crude product was then filtered through Celite and collected 0.73g (99%) of the desired product as a off-white solid. MS (ESI) m/z: 318.1 (M+H)+.

References:

WO2013/56060,2013,A1 Location in patent:Paragraph 00269

34784-04-8 Synthesis
5-Bromoisoquinoline

34784-04-8
354 suppliers
$7.00/1g

57260-71-6 Synthesis
1-BOC-Piperazine

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

tert-butyl 4-(isoquinolin-5-yl)piperazine-1-carboxylate

444620-69-3
22 suppliers
inquiry