{1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl ester

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Chemical Name:{1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl ester
CAS No.:221300-11-4
Molecular Formula:C₂₁H₂₃N₅O₄
Molecular Weight:409.445
Hs Code.:

Synonyms:{1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl ester

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Chemical Property of {1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl ester

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Technology Process of {1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl ester

There total 6 articles about {1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl 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: 66.0%

: 210036-03-6
[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-benzyloxycarbonylamino-acetic acid methyl ester

: 221300-11-4
{1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl ester

Guidance literature:: With lithium dihydrido borata-bicyclo[3.3.0]nonane; In tetrahydrofuran;
DOI:10.1016/S0960-894X(98)00672-6

Reference yield:

: 124676-23-9
α-(N-benzyloxycarbonyl)aminoglycine

: 221300-11-4
{1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / Et₃N / CHCl₃ / 11 h / Ambient temperature

2: 85 percent / K₂CO₃ / dimethylformamide

3: 65 percent / Zn, AcOH / ethanol

4: 66 percent / LiH*9-BBN / tetrahydrofuran

With potassium carbonate; acetic acid; triethylamine; lithium dihydrido borata-bicyclo[3.3.0]nonane; zinc; In tetrahydrofuran; ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(98)00672-6

Reference yield:

: 69195-96-6
5-nitro-1-(phenylmethyl)-1H-imidazole-4-carboxylic acid

: 221300-11-4
{1-[(5-Amino-1-benzyl-1H-imidazole-4-carbonyl)-amino]-2-hydroxy-ethyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / DCC, EtOAc / dimethylformamide / 3 h / 0 - 20 °C

2: 85 percent / Et₃N / CHCl₃ / 11 h / Ambient temperature

3: 85 percent / K₂CO₃ / dimethylformamide

4: 65 percent / Zn, AcOH / ethanol

5: 66 percent / LiH*9-BBN / tetrahydrofuran

With potassium carbonate; acetic acid; ethyl acetate; triethylamine; dicyclohexyl-carbodiimide; lithium dihydrido borata-bicyclo[3.3.0]nonane; zinc; In tetrahydrofuran; ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(98)00672-6