2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

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Chemical Name:2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester
CAS No.:901126-81-6
Molecular Formula:C₆₄H₈₂N₈O₁₄S
Molecular Weight:1219.47
Hs Code.:

2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

Synonyms:2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

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Chemical Property of 2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

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Technology Process of 2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

There total 8 articles about 2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl 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:

Reference yield: 77.0%

: Gly-Phe-Phe-NH₂

: 901126-80-5
2-[2-(2,6-bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-formyl-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

: 901126-81-6
2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

Guidance literature:: With sodium cyanoborohydride; acetic acid; In methanol; at 20 ℃; for 10h;
DOI:10.1021/ja061588y

Reference yield:

: 901126-73-6
3-hydroxy-2-mercaptobenzaldehyde

: 901126-81-6
2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: PPh₃; NCS / CH₂Cl₂ / 0.5 h / 0 °C

1.2: 58 percent / K₂CO₃ / CH₂Cl₂; dimethylformamide / 1 h / 0 °C

2.1: 83 percent / EDC; HOBt; DIEA / dimethylformamide / 12 h / 20 °C

3.1: 77 percent / AcOH; NaBH₃CN / methanol / 10 h / 20 °C

With N-chloro-succinimide; sodium cyanoborohydride; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja061588y

Reference yield:

: 901126-77-0
2-oxobenzo[d][1,3]oxathiole-4-carbaldehyde

: 901126-81-6
2-[2-((S)-2,6-Bis-tert-butoxycarbonylamino-hexanoylamino)-acetylamino]-3-phenyl-propionic acid 3-[({[(S)-1-((S)-1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methyl}-amino)-methyl]-2-(2,4,6-trimethoxy-benzylsulfanyl)-phenyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: aq. NaOH / methanol / 0.5 h / 20 °C

2.1: PPh₃; NCS / CH₂Cl₂ / 0.5 h / 0 °C

2.2: 58 percent / K₂CO₃ / CH₂Cl₂; dimethylformamide / 1 h / 0 °C

3.1: 83 percent / EDC; HOBt; DIEA / dimethylformamide / 12 h / 20 °C

4.1: 77 percent / AcOH; NaBH₃CN / methanol / 10 h / 20 °C

With sodium hydroxide; N-chloro-succinimide; sodium cyanoborohydride; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja061588y