(S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid

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Chemical Name:(S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid
CAS No.:107327-03-7
Molecular Formula:C₅₀H₆₂N₁₀O₁₃
Molecular Weight:1011.1
Hs Code.:

(S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid

Synonyms:(S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid

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Chemical Property of (S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid

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Technology Process of (S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid

There total 5 articles about (S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid 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:

: 107327-02-6
C₅₇H₆₈N₁₀O₁₃

: 107327-03-7
(S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide; for 12h;
DOI:10.1021/jm00389a002

Reference yield:

: 107327-00-4
(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carboxylic acid methyl ester

: 107327-03-7
(S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / 1N NaOH / methanol / a) 0 deg C, 2 h, b) RT, overnight

2: 84 percent / Et₃N, N-hydroxysuccinimide (HONSu), N,N'-dicyclohexylcarbodiimide (DCC) / dimethylformamide / a) 0 deg C, 1 h, b) RT, 48 h

3: H₂ / 10percent Pd/C / methanol; dimethylformamide / 12 h

With sodium hydroxide; 1-hydroxy-pyrrolidine-2,5-dione; hydrogen; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00389a002

Reference yield:

: 107326-99-8
Boc-Tyr-Asp-Gly-Trp-Lys-OCH₃

: 107327-03-7
(S)-3-{[(3S,9S,17S)-9-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-(1H-indol-3-ylmethyl)-2,5,8,11-tetraoxo-1,4,7,12-tetraaza-cycloheptadecane-17-carbonyl]-amino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 64 percent / DPPA, Et₃N / dimethylformamide / pH = 7-7.5; a) -25 deg C, 48 h, b) 4 deg C, 48 h

2: 72 percent / 1N NaOH / methanol / a) 0 deg C, 2 h, b) RT, overnight

3: 84 percent / Et₃N, N-hydroxysuccinimide (HONSu), N,N'-dicyclohexylcarbodiimide (DCC) / dimethylformamide / a) 0 deg C, 1 h, b) RT, 48 h

4: H₂ / 10percent Pd/C / methanol; dimethylformamide / 12 h

With sodium hydroxide; 1-hydroxy-pyrrolidine-2,5-dione; diphenyl-phosphinic acid; hydrogen; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00389a002