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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513Generated: October 23, 2026

3-Bromopyridine → tert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylate

https://huagongshe.com/en/reaction/513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant(R)-1-Boc-3-methylpiperazineHCID 2756811—
ReagentSodium t-butoxideHCID 23676156—
CatalystPalladium (II) acetateHCID 4144353—
Catalyst2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
SolventTolueneHCID 1140—
Producttert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylateHCID 89555981102.97%

Reaction Conditions

Temperature100 °C

Reaction Steps

_Repeat of reaction EN05798-78_ Diacetoxypalladium (0.112 g, 0.50 mmol) and dicyclohexyl(2',6'-diisopropoxybiphenyl-2-yl)phosphine (0.466 g, 1.00 mmol) were dissolved in toluene (15 mL) at ambient temperature under nitrogen. The mixture was degassed and purged with nitrogen several times and heated to 50°C for 20 mins. In a separate vessel, were mixed 3-bromopyridine (0.789 g, 4.99 mmol), sodium 2-methylpropan-2-olate (0.720 g, 7.49 mmol), (R)-tert-butyl 3-methylpiperazine-1-carboxylate (1g, 4.99 mmol) and toluene (10 mL). The mixture was degassed and purged with nitrogen several times. The catalyst mixture was added to the reaction vessel and the resulting mixture was degassed and purged with nitrogen, and heated at 100 °C under nitrogen overnight. The reaction mixture was filtered through celite, washing with EtOAc/MeOH. The filtrate was concentrated and the residue purified by flash silica chromatography, elution gradient 20 to 100% EtOAc in heptane. Pure fractions were evaporated to dryness to afford (R)-tert-butyl 3-methyl-4-(pyridin-3-yl)piperazine-1-carboxylate (1.426 g, 103 %) as a pale orange gum. [Rf ~ 0.1 in 1:1 EtOAc/hept] Note: Trace Ruphos contaminating product

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-b33a6a5e9f314a52b92d41be195f749c
Source note750 AstraZeneca ELN dataset