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(S)-2-(4-{[2-(2,4-Diamino-6,7-dihydro-5H-cyclopentapyrimidin-5-yl)-ethyl]-methyl-amino}-benzoylamino)-pentanedioic acid diethyl ester

Base Information
  • Chemical Name:(S)-2-(4-{[2-(2,4-Diamino-6,7-dihydro-5H-cyclopentapyrimidin-5-yl)-ethyl]-methyl-amino}-benzoylamino)-pentanedioic acid diethyl ester
  • CAS No.:1053636-20-6
  • Molecular Formula:C26H36N6O5
  • Molecular Weight:512.609
  • Hs Code.:
(S)-2-(4-{[2-(2,4-Diamino-6,7-dihydro-5H-cyclopentapyrimidin-5-yl)-ethyl]-methyl-amino}-benzoylamino)-pentanedioic acid diethyl ester

Synonyms:

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Chemical Property of (S)-2-(4-{[2-(2,4-Diamino-6,7-dihydro-5H-cyclopentapyrimidin-5-yl)-ethyl]-methyl-amino}-benzoylamino)-pentanedioic acid diethyl ester
Chemical Property:
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MSDS Files:
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Technology Process of (S)-2-(4-{[2-(2,4-Diamino-6,7-dihydro-5H-cyclopentapyrimidin-5-yl)-ethyl]-methyl-amino}-benzoylamino)-pentanedioic acid diethyl ester

There total 11 articles about (S)-2-(4-{[2-(2,4-Diamino-6,7-dihydro-5H-cyclopentapyrimidin-5-yl)-ethyl]-methyl-amino}-benzoylamino)-pentanedioic acid diethyl ester 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:
Multi-step reaction with 11 steps
1: 87 percent / N,N-diisopropylethylamine / dimethylformamide / 24 h / 70 °C
2: 63 percent / NaHCO3 / 1 h / 90 °C
3: 55 percent / 1N NaOH / ethanol
4: 95 percent / NaBH4
5: Et3N
6: 93 percent / NaI
7: Bu3SnH, AIBN / benzene / Heating
8: iso-Pr2EtN / methanol
9: 59 percent
10: 96 percent / 1N HCl / acetic acid
11: 1.) CDI, 2.) Et3N
With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; sodium hydrogencarbonate; triethylamine; N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole; sodium iodide; In methanol; ethanol; acetic acid; N,N-dimethyl-formamide; benzene;
DOI:10.1248/cpb.43.829
Guidance literature:
Multi-step reaction with 7 steps
1: Et3N
2: 93 percent / NaI
3: Bu3SnH, AIBN / benzene / Heating
4: iso-Pr2EtN / methanol
5: 59 percent
6: 96 percent / 1N HCl / acetic acid
7: 1.) CDI, 2.) Et3N
With hydrogenchloride; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; triethylamine; N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole; sodium iodide; In methanol; acetic acid; benzene;
DOI:10.1248/cpb.43.829
Guidance literature:
Multi-step reaction with 5 steps
1: Bu3SnH, AIBN / benzene / Heating
2: iso-Pr2EtN / methanol
3: 59 percent
4: 96 percent / 1N HCl / acetic acid
5: 1.) CDI, 2.) Et3N
With hydrogenchloride; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; triethylamine; N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole; In methanol; acetic acid; benzene;
DOI:10.1248/cpb.43.829
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