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154590-35-9

154590-35-9 Structure

154590-35-9 Structure
IdentificationBack Directory
[Name]

4-(4-Boc-piperazin-1-yl)-3-fluoroaniline
[CAS]

154590-35-9
[Synonyms]

4-(4-Boc-piperazin-1-yl)-3-fluoroaniline
4-(4-Amino-2-fluorophenyl)-1-Boc-piperazine
3-Fluoro-4-[4-(Boc-amino)piperidino]aniline
4-(4-Boc-piperazin-1-yl)-3-fluoroaniline ISO 9001:2015 REACH
4-(4-Amino-2-fluoro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
1-Piperazinecarboxylic acid, 4-(4-amino-2-fluorophenyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C15H22FN3O2
[MDL Number]

MFCD08443960
[MOL File]

154590-35-9.mol
[Molecular Weight]

295.35
Chemical PropertiesBack Directory
[Boiling point ]

439.6±45.0 °C(Predicted)
[density ]

1.198±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[form ]

solid
[pka]

6.67±0.10(Predicted)
[Appearance]

White to light yellow Solid
[InChI]

InChI=1S/C15H22FN3O2/c1-15(2,3)21-14(20)19-8-6-18(7-9-19)13-5-4-11(17)10-12(13)16/h4-5,10H,6-9,17H2,1-3H3
[InChIKey]

IULXQAJBODFBAK-UHFFFAOYSA-N
[SMILES]

N1(C(OC(C)(C)C)=O)CCN(C2=CC=C(N)C=C2F)CC1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P301+P312-P261
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

4-(4-Boc-piperazin-1-yl)-3-fluoroaniline(154590-35-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

tert-Butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate

154590-34-8

4-(4-Boc-piperazin-1-yl)-3-fluoroaniline

154590-35-9

Preparation of 3-4-2: [3-Fluoro-4-(Boc-piperazinyl)]aniline To 150 mL of ethyl acetate were sequentially added 9.3 g (28.6 mmol) of tert-butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate synthesized by the preparation of Example 3-4-1 and 930 mg (10 wt%) of Pd/C catalyst. The mixture was placed in a hydrogen reactor and reacted at 4 bar hydrogen pressure for 6 hours. Upon completion of the reaction, the Pd/C catalyst was removed by filtration. The filtrate was concentrated by distillation under reduced pressure and subsequently dried under vacuum at about 40 °C to give 8.22 g (yield: 97%) of the title compound. Mass spectrum (M + H)+: 296.11 1H-NMR (DMSO-d6) δ: 1.42 (s, 9H), 2.76 (br m, 4H), 3.43 (br m, 4H), 5.02 (s, 2H), 6.33 (m, 2H), 6.79 (m, 1H).

[References]

[1] Patent: US2011/306606, 2011, A1. Location in patent: Page/Page column 15
[2] Patent: EP2394993, 2011, A2. Location in patent: Page/Page column 23
[3] Patent: WO2005/82892, 2005, A2. Location in patent: Page/Page column 62-63
[4] Patent: WO2004/18439, 2004, A1. Location in patent: Page 31
[5] Patent: US2007/100141, 2007, A1. Location in patent: Page/Page column 27
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