(2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid

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Chemical Name:(2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid
CAS No.:147911-93-1
Molecular Formula:C₄₂H₄₈N₁₀O₈
Molecular Weight:820.905
Hs Code.:

(2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid

Synonyms:(2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid

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Chemical Property of (2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid

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Technology Process of (2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid

There total 11 articles about (2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic 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: 98.0%

: 147911-92-0
N^α-((tert-butyloxy)carbonyl)-N^β-<1-amino-3(S)-(4-amino-6-(amido-N^im-(triphenylmethyl)-erythro-β-hydroxy-L-histydyl methyl ester)-5-methylpyrimidin-2-yl)propion-3-yl>-(S)-β-aminoalanine amide

: 147911-93-1
(2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; methanol; water; at 0 ℃; for 1.5h;

Reference yield:

: 75452-30-1
pyrimidoblamic acid

: 147911-93-1
(2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / HOBt, EDCI / tetrahydrofuran; dimethylformamide / 72 h / 25 °C

2: 98 percent / 1 N aq. LiOH / tetrahydrofuran; methanol / 1.5 h / 0 °C

With lithium hydroxide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

Reference yield:

: 142582-33-0
erythro-N^?-Triphenylmethyl-β-hydroxy-L-histidinmethylester

: 147911-93-1
(2S,3R)-2-({6-Amino-2-[(S)-1-((S)-2-tert-butoxycarbonylamino-2-carbamoyl-ethylamino)-2-carbamoyl-ethyl]-5-methyl-pyrimidine-4-carbonyl}-amino)-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / HOBt, EDCI / tetrahydrofuran; dimethylformamide / 72 h / 25 °C

2: 98 percent / 1 N aq. LiOH / tetrahydrofuran; methanol / 1.5 h / 0 °C

With lithium hydroxide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;