3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric acid methyl ester

Base Information

Chemical Name:3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric acid methyl ester
CAS No.:897656-09-6
Molecular Formula:C₂₀H₂₇N₃O₄
Molecular Weight:373.452
Hs Code.:

3-(1-benzyl-1<i>H</i>-imidazol-4-yl)-2-<i>tert</i>-butoxycarbonylamino-butyric acid methyl ester

Synonyms:3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric acid methyl ester

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Chemical Property of 3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric acid methyl ester

Chemical Property:

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Technology Process of 3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric acid methyl ester

There total 5 articles about 3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric 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:

: 409102-42-7
(2S,3S)-2-Azido-3-(1-benzyl-1H-imidazol-4-yl)-butyric acid methyl ester

: 897656-09-6
3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂; acetic acid / Pd/C / methanol

2: CH₂Cl₂

With hydrogen; acetic acid; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1016/j.tet.2006.01.104

Reference yield:

: (S)-3-[(E)-3-(1-Benzyl-1H-imidazol-4-yl)-acryloyl]-4-phenyl-oxazolidin-2-one

: 897656-09-6
3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: CuBr*DMS / tetrahydrofuran / -40 °C

2.1: KHMDS / tetrahydrofuran / -50 °C

2.2: 72 percent / trisyl azide / tetrahydrofuran / -78 °C

3.1: 75 percent / NaOMe / CH₂Cl₂ / -10 °C

4.1: H₂; acetic acid / Pd/C / methanol

5.1: CH₂Cl₂

With copper(I) bromide dimethylsulfide complex; hydrogen; sodium methylate; potassium hexamethylsilazane; acetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.tet.2006.01.104

Reference yield:

: 409102-38-1
(S)-3-[(S)-3-(1-Benzyl-1H-imidazol-4-yl)-butyryl]-4-phenyl-oxazolidin-2-one

: 897656-09-6
3-(1-benzyl-1H-imidazol-4-yl)-2-tert-butoxycarbonylamino-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: KHMDS / tetrahydrofuran / -50 °C

1.2: 72 percent / trisyl azide / tetrahydrofuran / -78 °C

2.1: 75 percent / NaOMe / CH₂Cl₂ / -10 °C

3.1: H₂; acetic acid / Pd/C / methanol

4.1: CH₂Cl₂

With hydrogen; sodium methylate; potassium hexamethylsilazane; acetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.tet.2006.01.104