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Technology Process of (N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2

(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2

Base Information
  • Chemical Name:(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2
  • CAS No.:1515606-02-6
  • Molecular Formula:C92H128N12O18Si2
  • Molecular Weight:1746.27
  • Hs Code.:
(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)<sub>2</sub>

Synonyms:(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2

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Chemical Property of (N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2
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Technology Process of (N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2

There total 1 articles about (N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2 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:

Reference yield:

C<sub>58</sub>H<sub>106</sub>N<sub>10</sub>O<sub>14</sub>Si<sub>2</sub>
1515606-34-4

C58H106N10O14Si2

3-(benzyloxy)quinoline-2-carboxylic acid
110429-24-8

3-(benzyloxy)quinoline-2-carboxylic acid

(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)<sub>2</sub>
1515606-02-6

(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2

Guidance literature:
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 24h; Inert atmosphere;
DOI:10.1021/ol403319m

Reference yield: 87.0%

(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)<sub>2</sub>
1515606-02-6

(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-triisopropylsilyloxy-Pip-Gly-Sar-N-Me-L-Val)2

(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-hydroxy-Pip-Gly-Sar-N-Me-L-Val)<sub>2</sub>
1515606-05-9

(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-hydroxy-Pip-Gly-Sar-N-Me-L-Val)2

Guidance literature:
With hydrogen fluoride; In dichloromethane; at 0 - 20 ℃; for 72h; Inert atmosphere;
DOI:10.1021/ol403319m
upstream raw materials:

C58H106N10O14Si2

3-(benzyloxy)quinoline-2-carboxylic acid

Downstream raw materials:

(N-[(3-benzyloxy)quinolyl]-2-carbonyl-D-Ser-(S)-β-L-hydroxy-Pip-Gly-Sar-N-Me-L-Val)2

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