[1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

Base Information

Chemical Name:[1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester
CAS No.:340732-83-4
Molecular Formula:C₂₉H₃₅N₃O₈
Molecular Weight:553.612
Hs Code.:

[1-(benzyloxycarbonylamino-phenyl-acetyl)-4-<i>tert</i>-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

Synonyms:[1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of [1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

Chemical Property:

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Technology Process of [1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

There total 1 articles about [1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic 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:

Reference yield:

: 5491-18-9,17609-52-8,53990-33-3,60584-76-1
(S)-N-(benzyloxycarbonyl)phenylglycine

: 169157-67-9
(S)-3-methoxycarbonylmethyl-2-oxopiperazine-1-acetic acid tert-butyl ester

: 340732-83-4
[1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1248/cpb.49.258

Reference yield:

: 340732-83-4
[1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

: [1-(amino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; for 0.666667h;
DOI:10.1248/cpb.49.258

Reference yield:

: 340732-83-4
[1-(benzyloxycarbonylamino-phenyl-acetyl)-4-tert-butoxycarbonylmethyl-3-oxo-piperazin-2-yl]-acetic acid methyl ester

: {4-[(4-carbamimidoyl-benzoylamino)-phenyl-acetyl]-3-methoxycarbonylmethyl-2-oxo-piperazin-1-yl}-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / 10 percent Pd/C / methanol / 0.67 h / 20 °C

2: NaHCO₃ / H₂O; dioxane / 1.5 h / 20 °C

3: trifluoroacetic acid / toluene / 1 h / 20 °C

With hydrogen; sodium hydrogencarbonate; trifluoroacetic acid; palladium on activated charcoal; In 1,4-dioxane; methanol; water; toluene;
DOI:10.1248/cpb.49.258