ChemicalBook CAS DataBase List 3-PYRIDYLAMINE, N-(1-METHYLETHYL)-2-(1-PIPERAZINYL)-,DIHYDROCHLORIDE MONOHYDRATE

3-PYRIDYLAMINE, N-(1-METHYLETHYL)-2-(1-PIPERAZINYL)-,DIHYDROCHLORIDE MONOHYDRATE synthesis

5synthesis methods

Product Name:3-PYRIDYLAMINE, N-(1-METHYLETHYL)-2-(1-PIPERAZINYL)-,DIHYDROCHLORIDE MONOHYDRATE
CAS Number:147539-21-7
Molecular formula:C12H20N4
Molecular Weight:220.31

136818-14-9 Synthesis

1-((1,1-DIMETHYLETHOXY)CARBONYL)-4-(3-((1-METHYLETHYL)AMINO)-2-PYRIDYL)PIPERAZINE

136818-14-9
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3-PYRIDYLAMINE, N-(1-METHYLETHYL)-2-(1-PIPERAZINYL)-,DIHYDROCHLORIDE MONOHYDRATE

147539-21-7
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Yield:147539-21-7 100%

Reaction Conditions:

with trifluoroacetic acid in dichloromethane at 0 - 20; for 24.75 h;

Steps:

1 Synthesis of mPEGn-O-Delavirdine Conjugates

Trifluoroacetic acid (2.0 mL) was added to a stirred solution of 2-(Boc-piperazinyl)-3-(i -propylamino)pyridine 4 (1.426 g, 4.45 mmol) in dichloromethane (10 mL) at 0° C.
The resulting mixture was stirred at 0° C. for 30 min, at room temperature for 1 h 15 min.
Additional quantities of TFA (2.0 mL) were added.
The mixture was stirred at room temperature for another 23 h. Sat.
K₂CO₃ solution was slowly added to quench the reaction (gas ↑).
Small amount of water was added to help the layers separation.
The organic phase was separated and the aqueous phase was extracted with dichloromethane (2*25 mL).
The combined organic solution was washed with brine, dried over anhydrous Na₂SO₄, and concentrated to afford the product in quantitative yield. ¹H-NMR (CDCl₃): 7.681 (dd, J=5.0 Hz and 1.5 Hz, 1 H, Ar-H), 6.890 (dd, J=8.0 Hz and 5.0 Hz, 1 H, Ar-H), 6.800 (dd, J=8.0 Hz and 1.5 Hz, 1 H, Ar-H), 4.170 (d, J=7.5 Hz, 1 H, NH), 3.567-3.485 (m, 1 H, CH), 3.046 (s, 8 H, 4 CH₂), 1.983 (br, 1 H, NH), 1.234 (d, J=6.0 Hz, 6 H, 2 CH₃).