Hydrochloric Acid → 1-[2-(4-Nitrophenyl)ethyl]-4-[2-(4-nitrophenyl)propyl]piperazine

HRID 1519568Notizen

Reaktionsgleichung

[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][N:12]2[CH2:17][CH2:16][N:15]([C:18](=O)[CH:19]([C:21]3[CH:26]=[CH:25][C:24]([N+:27]([O-:29])=[O:28])=[CH:23][CH:22]=3)[CH3:20])[CH2:14][CH2:13]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].Cl.[OH-].[Na+]>C1COCC1>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][N:12]2[CH2:13][CH2:14][N:15]([CH2:18][CH:19]([C:21]3[CH:22]=[CH:23][C:24]([N+:27]([O-:29])=[O:28])=[CH:25][CH:26]=3)[CH3:20])[CH2:16][CH2:17]2)=[CH:6][CH:5]=1)([O-:3])=[O:2]

Komponenten

Reaktionsbedingungen

Temperatur: 65 °C

Versuchsvorschrift

Borane tetrahydrofuran complex 1M (0.714 ml, 0.714 mmol) was added to a stirred solution of 1-[2-(4-nitrophenyl)ethyl]-4-[2-(4-nitrophenyl)propanoyl]piperazine (92 mg, 0.22 mmol) in THF then refluxed for 1 hr. LC-MS and TLC showed starting material left. More borane-THF complex 1M (0.71 ml, 0.71 mmol) was added to the reaction and refluxed for 5 hrs. The reaction was cooled and added 6N HCl and then warmed to 65° C. for 0.5 hour. The reaction was poured into 1N NaOH and extracted with ethyl acetate. The ethyl acetate layer was washed with water and brine then dried and concentrated. The residue was purified by mass directed HPLC. LC-MS (IE, m/z): 399 [M+1]+. (0.34 μM)

Aufarbeitung

temperaturethen refluxed for 1 hr
waitleft
additionMore borane-THF complex 1M (0.71 ml, 0.71 mmol) was added to the reaction
temperaturerefluxed for 5 hrs
temperatureThe reaction was cooled
extractionextracted with ethyl acetate
washThe ethyl acetate layer was washed with water and brine
customthen dried
concentrationconcentrated
customThe residue was purified by mass

Quellen und Nachweise

ORD-Eintrag: ord-e2dc9832342146f78d5bd6801be6f079
Quelldatensatz: uspto-grants-2015_07
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US09073882B2

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