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(S)-2-[(S)-2-((S)-2-Amino-propionyloxy)-3-methyl-butyrylamino]-5-[4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid tert-butyl ester

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  • Chemical Name:(S)-2-[(S)-2-((S)-2-Amino-propionyloxy)-3-methyl-butyrylamino]-5-[4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid tert-butyl ester
  • CAS No.:204329-91-9
  • Molecular Formula:C25H35F3N4O5
  • Molecular Weight:528.572
  • Hs Code.:
  • Mol file:204329-91-9.mol
(S)-2-[(S)-2-((S)-2-Amino-propionyloxy)-3-methyl-butyrylamino]-5-[4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid tert-butyl ester

Synonyms:(S)-2-[(S)-2-((S)-2-Amino-propionyloxy)-3-methyl-butyrylamino]-5-[4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid tert-butyl ester

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Chemical Property of (S)-2-[(S)-2-((S)-2-Amino-propionyloxy)-3-methyl-butyrylamino]-5-[4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid tert-butyl ester Edit
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Technology Process of (S)-2-[(S)-2-((S)-2-Amino-propionyloxy)-3-methyl-butyrylamino]-5-[4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid tert-butyl ester

There total 21 articles about (S)-2-[(S)-2-((S)-2-Amino-propionyloxy)-3-methyl-butyrylamino]-5-[4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-pentanoic acid tert-butyl 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 3 steps
1: 94 percent / H2 / 10percent Pd/C / methanol; H2O
2: 91 percent / DCC, HOBt, NMM / tetrahydrofuran
3: 57 percent / 3M HCl / ethyl acetate; propan-2-ol
With 4-methyl-morpholine; hydrogenchloride; hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; water; ethyl acetate; isopropyl alcohol;
DOI:10.1246/cl.1998.203
Guidance literature:
Multi-step reaction with 17 steps
1: imidazole / dimethylformamide
2: 79 percent / 1.) n-BuLi / diethyl ether / -42 °C / 1.) -42 -> 0 deg C
3: 91 percent / NH2OH*HCl, Et3N / ethanol / Heating
4: 98 percent / pyridine / 0 deg C -> room temp.
5: 98 percent / liq. NH3 / diethyl ether / -78 -> -33 deg C -> room temp.
6: 1.) t-BuOCl; 2.) Et3N / 1.) Et2O, -50 deg C; 2.) Et2O, -50 deg C -> room temp.
7: CSA / methanol
8: 95 percent / CBr4, PPh3 / toluene
9: 75 percent / NaH / dimethylformamide
10: 3M NaOH / ethanol
11: 95 percent / dioxane / 80 °C
12: 26 percent / acylase, CoCl2 / H2O / pH = 7.0
13: 97 percent / Et3N / dioxane; H2O
14: 71 percent / CH2Cl2 / Heating
15: 73 percent / 3M HCl / ethyl acetate; H2O
16: 91 percent / DCC, HOBt, NMM / tetrahydrofuran
17: 57 percent / 3M HCl / ethyl acetate; propan-2-ol
With 4-methyl-morpholine; pyridine; 1H-imidazole; hydrogenchloride; sodium hydroxide; n-butyllithium; acylase; tert-butylhypochlorite; carbon tetrabromide; camphor-10-sulfonic acid; hydroxylamine hydrochloride; ammonia; sodium hydride; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; ethanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; toluene;
DOI:10.1246/cl.1998.203
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