149376-69-2

  • Product Name:Boc-PNA-A(Z)-OH
  • Molecular Formula:C24H29N7O7
  • Molecular Weight:527.53000
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Product Details

Purity:99%

Manufacturer Sells Best Quality Boc-PNA-A(Z)-OH 149376-69-2 with stock

  • Molecular Formula:C24H29N7O7
  • Molecular Weight:527.53000
  • PSA:177.87000 
  • LogP:2.47680 

149376-69-2 Relevant articles

Synthesis of Peptide Nucleic Acid Monomers Containing the Four Natural Nucleobases: Thymine, Cytosine, Adenine, and Guanine and Their Oligomerization

Dueholm, Kim L.,Egholm, Michael,Behrens, Carsten,Christensen, Leif,Hansen, Henrik F.,et al.

, p. 5767 - 5773 (2007/10/02)

The preparation of mixed-sequence PNAs (...

Peptide Nucleic Acids containing Adenine or Guanine recognize Thymine and Cytosine in Complementary DNA Sequences

Egholm, Michael,Behrens, Carsten,Christensen, Leif,Berg, Rolf H.,Nielsen, Peter E.,Buchardt, Ole

, p. 800 - 801 (2007/10/02)

Peptide nucleic acid (PNA) monomer build...

149376-69-2 Process route

ethyl N-((N<sup>6</sup>-(benzyloxycarbonyl)adenin-9-yl)acetyl)-N-(2-Boc-aminoethyl)glycinate
149376-68-1

ethyl N-((N6-(benzyloxycarbonyl)adenin-9-yl)acetyl)-N-(2-Boc-aminoethyl)glycinate

N-((N<sup>6</sup>-(benzyloxycarbonyl)adenin-9-yl)acetyl)-N-(2-Boc-aminoethyl)glycine
149376-69-2

N-((N6-(benzyloxycarbonyl)adenin-9-yl)acetyl)-N-(2-Boc-aminoethyl)glycine

Conditions
Conditions Yield
With lithium hydroxide; In tetrahydrofuran; at 0 ℃; for 0.25h;
55%
With sodium hydroxide; water; In methanol;
ethyl 2-(9H-adenin-9-yl)acetate
25477-96-7

ethyl 2-(9H-adenin-9-yl)acetate

N-((N<sup>6</sup>-(benzyloxycarbonyl)adenin-9-yl)acetyl)-N-(2-Boc-aminoethyl)glycine
149376-69-2

N-((N6-(benzyloxycarbonyl)adenin-9-yl)acetyl)-N-(2-Boc-aminoethyl)glycine

Conditions
Conditions Yield
Multi-step reaction with 4 steps
1: 63 percent / dimethylformamide; CH2Cl2 / 24 h
2: aq. NaOH / methanol / 0.5 h / 0 °C
3: 3,4-dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine, DCC / CH2Cl2; dimethylformamide / 1.) 0 deg C, 2.5 h, 2.) r.t., 1.5 h
4: 55 percent / 1 M aq. LiOH / tetrahydrofuran / 0.25 h / 0 °C
With lithium hydroxide; sodium hydroxide; 3-hydroxy-3,4-dihydrobenzotriazine-4-one; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
Multi-step reaction with 4 steps
1: dimethylformamide; CH2Cl2
2: LiOH, H2O / tetrahydrofuran
3: dicyclohexylcarbodiimide (DCC), DhbtOH / dimethylformamide; CH2Cl2
4: NaOH, H2O / methanol
With lithium hydroxide; sodium hydroxide; water; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

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