2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester

Base Information

• Chemical Name: 2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester
• CAS No.: 207235-71-0
• Molecular Formula: C₂₆H₂₄N₂O₆
• Molecular Weight: 460.486

Synonyms:2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester

Chemical Property of 2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester

Chemical Property:

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Technology Process of 2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester

There total 3 articles about 2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic 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:

N-benzyloxycarbonyl-2-amino-3-phenylpropionaldehyde (59830-60-3,63219-70-5,68474-26-0) → 2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester (207235-71-0)

Guidance literature:

Multi-step reaction with 3 steps

1: 94 percent / Et₃N / CH₂Cl₂ / 4 h / 20 °C

2: HCl / CHCl₃ / 3 h / 0 °C

3: ethanol / 6 h / Heating

With hydrogenchloride; triethylamine; In ethanol; dichloromethane; chloroform;

DOI:10.1021/jm000496v

Reference yield:

3-(benzyloxycarbonyl)amino-2-hydroxy-4-phenylbutanenitrile (66413-45-4) → 2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester (207235-71-0)

Guidance literature:

Multi-step reaction with 2 steps

1: HCl / CHCl₃ / 3 h / 0 °C

2: ethanol / 6 h / Heating

With hydrogenchloride; In ethanol; chloroform;

DOI:10.1021/jm000496v

Reference yield:

3-hydroxy-4-aminobenzoic acid methyl ester (63435-16-5) + 3-benzyloxycarbonylamino-2-hydroxy-4-phenyl-butyrimidic acid ethyl ester; hydrochloride → 2-(2-benzyloxycarbonylamino-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester (207235-71-0)

Guidance literature:

In ethanol; for 6h; Heating;

DOI:10.1021/jm000496v

upstream raw materials:

3-hydroxy-4-aminobenzoic acid methyl ester

N-benzyloxycarbonyl-2-amino-3-phenylpropionaldehyde

3-(benzyloxycarbonyl)amino-2-hydroxy-4-phenylbutanenitrile

Downstream raw materials:

2-[5-benzyloxycarbonylamino-2-(4-fluorophenyl)-6-oxo-1,6-dihydro-1-pyrimidinyl]-N-[1-[[6-(methoxycarbonyl)benzoxazol-2-yl]carbonyl]-2-phenylethyl]acetamide

2-(2-{2-[5-benzyloxycarbonylamino-2-(4-fluoro-phenyl)-6-oxo-6H-pyrimidin-1-yl]-acetylamino}-1-hydroxy-3-phenyl-propyl)-benzooxazole-6-carboxylic acid methyl ester

2-amino-1-hydroxy-1-[6-(methoxycarbonyl)benzoxazol-2-yl]-3-phenylpropane

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