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2-({(S)-2-[(2-{6-Benzyloxymethyl-2-[2-((S)-1-tert-butoxycarbonylamino-ethyl)-5-methyl-oxazol-4-yl]-pyridin-3-yl}-thiazole-4-carbonyl)-amino]-3-methyl-butyrylamino}-methyl)-5-methyl-oxazole-4-carboxylic acid methyl ester

Base Information
  • Chemical Name:2-({(S)-2-[(2-{6-Benzyloxymethyl-2-[2-((S)-1-tert-butoxycarbonylamino-ethyl)-5-methyl-oxazol-4-yl]-pyridin-3-yl}-thiazole-4-carbonyl)-amino]-3-methyl-butyrylamino}-methyl)-5-methyl-oxazole-4-carboxylic acid methyl ester
  • CAS No.:271597-68-3
  • Molecular Formula:C40H47N7O9S
  • Molecular Weight:801.921
  • Hs Code.:
2-({(S)-2-[(2-{6-Benzyloxymethyl-2-[2-((S)-1-tert-butoxycarbonylamino-ethyl)-5-methyl-oxazol-4-yl]-pyridin-3-yl}-thiazole-4-carbonyl)-amino]-3-methyl-butyrylamino}-methyl)-5-methyl-oxazole-4-carboxylic acid methyl ester

Synonyms:2-({(S)-2-[(2-{6-Benzyloxymethyl-2-[2-((S)-1-tert-butoxycarbonylamino-ethyl)-5-methyl-oxazol-4-yl]-pyridin-3-yl}-thiazole-4-carbonyl)-amino]-3-methyl-butyrylamino}-methyl)-5-methyl-oxazole-4-carboxylic acid methyl ester

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Chemical Property of 2-({(S)-2-[(2-{6-Benzyloxymethyl-2-[2-((S)-1-tert-butoxycarbonylamino-ethyl)-5-methyl-oxazol-4-yl]-pyridin-3-yl}-thiazole-4-carbonyl)-amino]-3-methyl-butyrylamino}-methyl)-5-methyl-oxazole-4-carboxylic acid methyl ester
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Technology Process of 2-({(S)-2-[(2-{6-Benzyloxymethyl-2-[2-((S)-1-tert-butoxycarbonylamino-ethyl)-5-methyl-oxazol-4-yl]-pyridin-3-yl}-thiazole-4-carbonyl)-amino]-3-methyl-butyrylamino}-methyl)-5-methyl-oxazole-4-carboxylic acid methyl ester

There total 22 articles about 2-({(S)-2-[(2-{6-Benzyloxymethyl-2-[2-((S)-1-tert-butoxycarbonylamino-ethyl)-5-methyl-oxazol-4-yl]-pyridin-3-yl}-thiazole-4-carbonyl)-amino]-3-methyl-butyrylamino}-methyl)-5-methyl-oxazole-4-carboxylic acid methyl 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 17 steps
1: 80 percent / dirhodium(II) acetate / CHCl3 / Heating
2: 70 percent / triethylamine; triphenylphosphine; iodine / CH2Cl2 / 20 °C
3: 95 percent / aq. LiOH / methanol / 5 h / 20 °C
4: triethylamine / tetrahydrofuran / 0.33 h / 0 °C
5: tetrahydrofuran / 20 °C
6: 85 percent / ammonium acetate / benzene; acetic acid / 24 h / Heating
7: ethanol / 50 °C
8: 0.5 h / 140 °C
9: 92 percent / aq. LiOH / tetrahydrofuran / 20 - 45 °C
10: triethylamine / tetrahydrofuran / 0.83 h / -10 °C
11: 32percent aq. NH4OH / tetrahydrofuran / 0.75 h / -10 °C
12: 59 percent / Lawesson's reagent / benzene / 5 h / Heating
13: potassium hydrogen carbonate / tetrahydrofuran / 16 h / -3 °C
14: trifluoroacetic anhydride; 2,6-lutidine / tetrahydrofuran / 3 h / 0 °C
15: 94 percent / aq. LiOH / tetrahydrofuran / 20 °C
16: N-methylmorpholine / tetrahydrofuran / 0.5 h / 0 °C
17: tetrahydrofuran / 1 h / 0 °C
With Lawessons reagent; 4-methyl-morpholine; 2,6-dimethylpyridine; ammonium acetate; lithium hydroxide; iodine; potassium hydrogencarbonate; triethylamine; triphenylphosphine; trifluoroacetic anhydride; dirhodium tetraacetate; In tetrahydrofuran; methanol; ethanol; dichloromethane; chloroform; acetic acid; benzene; 1: Condensation / 2: Cyclization / 3: Hydrolysis / 4: Carboxylation / 5: Substitution / 6: Amination / 7: Condensation / 8: Cyclization / 9: Hydrolysis / 10: Carboxylation / 11: Amination / 12: Substitution / 13: Condensation / 14: Cyclization / 15: Hydrolysis / 16: Carboxylation / 17: Substitution;
DOI:10.1021/ja994247b
Guidance literature:
Multi-step reaction with 4 steps
1: 100 percent / H2 / 10percent Pd/C / methanol / 4 h / 20 °C / 760.05 Torr
2: tetrahydrofuran / 1 h / 0 °C
3: 100 percent / acetyl chloride / methanol / 20 °C
4: tetrahydrofuran / 1 h / 0 °C
With hydrogen; acetyl chloride; 10percent Pd/C; In tetrahydrofuran; methanol; 1: Catalytic hydrogenation / 2: Substitution / 3: Deprotection / 4: Substitution;
DOI:10.1021/ja994247b
Guidance literature:
Multi-step reaction with 4 steps
1: N-methylmorpholine / tetrahydrofuran / 0.33 h / -10 °C
2: tetrahydrofuran / 1 h / 0 °C
3: 100 percent / acetyl chloride / methanol / 20 °C
4: tetrahydrofuran / 1 h / 0 °C
With 4-methyl-morpholine; acetyl chloride; In tetrahydrofuran; methanol; 1: Carboxylation / 2: Substitution / 3: Deprotection / 4: Substitution;
DOI:10.1021/ja994247b
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