tert-Butyl piperazine-1-carboxylate → HCID 130471524, compound

HRID 646Notes

Reaction equation

HRID 646 reaction equation
CC(C)(C)OC(=O)N1CCNCC1.COC(=O)c1cc(F)cc(Br)c1>C1CCOC1.CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC(C)c1cc(C(C)C)c(-c2ccccc2P(C2CCCCC2)C2CCCCC2)c(C(C)C)c1.[Na+].[Pd]>CC(C)(C)OC(=O)N1CCN(c2cc(F)cc(C(=O)O)c2)CC1

Participants

7

Conditions

Temperature
80 °C

Procedure

To methyl 3-bromo-5-fluorobenzoate (1.5 g, 6.44 mmol) dissolved in dry THF (20 mL) was added tert-butyl piperazine-1-carboxylate (1.199 g, 6.44 mmol), Sodium-t-butoxide (1.856 g, 19.31 mmol) and purged with N2 gas for 10 min followed by the addition of2-(Dicyclohexylphosphino)-2',4',6'-tri-i- propyl-1,1'-biphenyl (0.307 g, 0.64 mmol), Palladium II acetate (0.145 g, 0.64 mmol) . The contents were further purged with N2 gas for further 10 min and heated at 85 °C for overnight. The reaction mass was concentrated and the reside diluted with water and extracted with ethyl acetate . The combined organic extracts were washed with brine solution and dried over anhydrous sodium sulphate. The organic layer was evaporated under reduced pressure to obtain the crude product which was purified by 60-120 mesh silica gel column chromatography using 25% Ethyl acetate ; hexanes mixture to obtain 3-(4-(tert- butoxycarbonyl)piperazin-1-yl)-5-fluorobenzoic acid (1.500 g, 71.8 %) an oil. m/z (ES-), M- = 323

Sources & evidence

ORD record
ord-d16088bf6acb4600ad776547cf486a02
Source dataset
750 AstraZeneca ELN dataset
Original link
View source

Reaction notes

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