3-Bromopyridine → Tert-butyl 4-(pyridin-3-YL)piperazine-1-carboxylate

HRID 608

Reaction equation

HRID 608 reaction equation
Brc1cccnc1.CC(C)(C)OC(=O)N1CCNCC1>C1COCCO1.CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC(C)Oc1cccc(OC(C)C)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1.[Na+].[Pd]>CC(C)(C)OC(=O)N1CCN(c2cccnc2)CC1

Participants

7

Conditions

Temperature
100 °C

Procedure

diacetoxypalladium (0.072 g, 0.32 mmol) and RuPhos (0.301 g, 0.64 mmol) were stirred in 1,4-dioxane (11.36 ml) for 10 mins at 50 °C.tert-butyl piperazine-1-carboxylate (0.6 g, 3.22 mmol), 3-bromopyridine (0.310 ml, 3.22 mmol) and sodium tert-butoxide (0.464 g, 4.83 mmol) were added and the reaction mixture was stirred at 100 °C for 64 h. The reaction mixture was filtered through celite. The crude product was purified by flash silica chromatography, elution gradient 20 to 100% EtOAc in heptane. Pure fractions were evaporated to dryness to afford tert-butyl 4-(pyridin-3-yl)piperazine-1-carboxylate (0.322 g, 38.0 %) as a yellow oil which crystallised on standing. This was then combined with EN06111-39-01.

Sources & evidence

ORD record
ord-c9d3e32c4ae3434fab0938e5982b9ebd
Source dataset
750 AstraZeneca ELN dataset
Original link
View source

Linked notes

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