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2(S)-[2(S)-benzyloxymethyl-3-methylbutyl]-3,6-diethoxy-2,5-dihydro-pyrazine

Base Information Edit
  • Chemical Name:2(S)-[2(S)-benzyloxymethyl-3-methylbutyl]-3,6-diethoxy-2,5-dihydro-pyrazine
  • CAS No.:172900-78-6
  • Molecular Formula:C21H32N2O3
  • Molecular Weight:360.497
  • Hs Code.:
  • DSSTox Substance ID:DTXSID401125817
  • Mol file:172900-78-6.mol
2(S)-[2(S)-benzyloxymethyl-3-methylbutyl]-3,6-diethoxy-2,5-dihydro-pyrazine

Synonyms:SCHEMBL8904641;NKWXKUZEASCOPC-MOPGFXCFSA-N;DTXSID401125817;(2S)-3,6-Diethoxy-2,5-dihydro-2-[(2S)-3-methyl-2-[(phenylmethoxy)methyl]butyl]pyrazine;2(S)-[2(S)-benzyloxymethyl-3-methylbutyl]-3,6-diethoxy-2,5-dihydro-pyrazine;172900-78-6

Suppliers and Price of 2(S)-[2(S)-benzyloxymethyl-3-methylbutyl]-3,6-diethoxy-2,5-dihydro-pyrazine
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Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2(S)-[2(S)-benzyloxymethyl-3-methylbutyl]-3,6-diethoxy-2,5-dihydro-pyrazine Edit
Chemical Property:
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:11
  • Exact Mass:360.24129289
  • Heavy Atom Count:26
  • Complexity:456
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCOC1=NC(C(=NC1)OCC)CC(COCC2=CC=CC=C2)C(C)C
  • Isomeric SMILES:CCOC1=N[C@H](C(=NC1)OCC)C[C@H](COCC2=CC=CC=C2)C(C)C
Technology Process of 2(S)-[2(S)-benzyloxymethyl-3-methylbutyl]-3,6-diethoxy-2,5-dihydro-pyrazine

There total 6 articles about 2(S)-[2(S)-benzyloxymethyl-3-methylbutyl]-3,6-diethoxy-2,5-dihydro-pyrazine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
(2S)-(benzyloxymethyl)-3-methyl-butyl bromide; With n-butyllithium; In tetrahydrofuran; at -40 ℃;
(2R)-2,5-dihydro-2-isopropyl-3,6-dimethoxypyrazine; In tetrahydrofuran; at -40 - -18 ℃; for 16h; Title compound not separated from byproducts;
DOI:10.1002/hlca.200390235
Guidance literature:
Multi-step reaction with 5 steps
1.1: TiCl4; Huenig'base / CH2Cl2 / 1 h / 0 °C
1.2: 50 percent / CH2Cl2 / 20 h / 0 °C
2.1: H2O2; LiOH / tetrahydrofuran; H2O / 0 - 2 °C
2.2: 92 percent / tetrahydrofuran; H2O / 16 h / 20 °C
3.1: NaBH4 / tetrahydrofuran / 0.67 h / 10 - 20 °C
3.2: I2 / tetrahydrofuran / 72 h / 20 °C
3.3: 92 percent / tetrahydrofuran; methanol / 1 h / 20 °C
4.1: 70 percent / Ph3P; NBS / 20 °C
5.1: BuLi / tetrahydrofuran / -40 °C
5.2: tetrahydrofuran / 16 h / -40 - -18 °C
With lithium hydroxide; sodium tetrahydroborate; N-Bromosuccinimide; n-butyllithium; dihydrogen peroxide; titanium tetrachloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1002/hlca.200390235
Guidance literature:
Multi-step reaction with 5 steps
1.1: TiCl4; Huenig'base / CH2Cl2 / 1 h / 0 °C
1.2: 50 percent / CH2Cl2 / 20 h / 0 °C
2.1: H2O2; LiOH / tetrahydrofuran; H2O / 0 - 2 °C
2.2: 92 percent / tetrahydrofuran; H2O / 16 h / 20 °C
3.1: NaBH4 / tetrahydrofuran / 0.67 h / 10 - 20 °C
3.2: I2 / tetrahydrofuran / 72 h / 20 °C
3.3: 92 percent / tetrahydrofuran; methanol / 1 h / 20 °C
4.1: 70 percent / Ph3P; NBS / 20 °C
5.1: BuLi / tetrahydrofuran / -40 °C
5.2: tetrahydrofuran / 16 h / -40 - -18 °C
With lithium hydroxide; sodium tetrahydroborate; N-Bromosuccinimide; n-butyllithium; dihydrogen peroxide; titanium tetrachloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1002/hlca.200390235
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