[3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

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Chemical Name:[3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium
CAS No.:176752-34-4
Molecular Formula:C₄₉H₆₀N₉O₆S₃
Molecular Weight:967.27
Hs Code.:

[3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

Synonyms:[3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

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Chemical Property of [3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

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Technology Process of [3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

There total 9 articles about [3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium 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: 68.0%

: 176752-33-3
[3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-tert-Butoxycarbonylamino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

: 176752-34-4
[3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

Guidance literature:: With hydrogenchloride; acetic acid; at 25 ℃; for 0.0833333h;
DOI:10.1016/0968-0896(95)00183-2

Reference yield:

: 76-83-5
trityl chloride

: 176752-34-4
[3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

Guidance literature:: Multi-step reaction with 6 steps

1: 99 percent / Et₃N / benzene / 1 h / 80 °C

2: 0.78 g / H₂ / 10percent Pd/C / methanol / 2.5 h / 25 °C / 760 Torr

3: 98 percent / aq. NaHCO₃ / tetrahydrofuran / 2 h / 25 °C

4: 85 percent / 0.1 N aq. LiOH / methanol / 2 h / 4 °C

5: 77 percent / DCC, HOBt, NaHCO₃ / dimethylformamide / 12 h / 25 °C

6: 68 percent / aq. HCl, AcOH / 0.08 h / 25 °C

With hydrogenchloride; lithium hydroxide; hydrogen; sodium hydrogencarbonate; benzotriazol-1-ol; acetic acid; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; benzene;
DOI:10.1016/0968-0896(95)00183-2

Reference yield:

: 40917-50-8
1,N^α-bis-benzyloxycarbonyl-histidine methyl ester

: 176752-34-4
[3-({2'-[2-((2S,3R)-2-{(2S,3S,4R)-4-[(S)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)-propionylamino]-3-hydroxy-2-methyl-pentanoylamino}-3-hydroxy-butyrylamino)-ethyl]-[2,4']bithiazolyl-4-carbonyl}-amino)-propyl]-dimethyl-sulfonium

Guidance literature:: Multi-step reaction with 7 steps

1: 80 percent / 1N aq. NaOH / methanol / 0.01 h / -20 °C

2: 99 percent / Et₃N / benzene / 1 h / 80 °C

3: 0.78 g / H₂ / 10percent Pd/C / methanol / 2.5 h / 25 °C / 760 Torr

4: 98 percent / aq. NaHCO₃ / tetrahydrofuran / 2 h / 25 °C

5: 85 percent / 0.1 N aq. LiOH / methanol / 2 h / 4 °C

6: 77 percent / DCC, HOBt, NaHCO₃ / dimethylformamide / 12 h / 25 °C

7: 68 percent / aq. HCl, AcOH / 0.08 h / 25 °C

With hydrogenchloride; lithium hydroxide; sodium hydroxide; hydrogen; sodium hydrogencarbonate; benzotriazol-1-ol; acetic acid; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; benzene;
DOI:10.1016/0968-0896(95)00183-2