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

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Chemical Name:2-{2-[2-(5-benzyloxycarbonylamino-6-oxo-2-pyridin-4-yl-6H-pyrimidin-1-yl)-acetylamino]-1-hydroxy-3-phenyl-propyl}-benzooxazole-5-carboxylic acid methyl ester
CAS No.:1060718-86-6
Molecular Formula:C₃₇H₃₂N₆O₈
Molecular Weight:688.696
Hs Code.:

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

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

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

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

There total 6 articles about 2-{2-[2-(5-benzyloxycarbonylamino-6-oxo-2-pyridin-4-yl-6H-pyrimidin-1-yl)-acetylamino]-1-hydroxy-3-phenyl-propyl}-benzooxazole-5-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:

: 59830-60-3,63219-70-5,68474-26-0
N-benzyloxycarbonyl-2-amino-3-phenylpropionaldehyde

: 1060718-86-6
2-{2-[2-(5-benzyloxycarbonylamino-6-oxo-2-pyridin-4-yl-6H-pyrimidin-1-yl)-acetylamino]-1-hydroxy-3-phenyl-propyl}-benzooxazole-5-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

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

2: HCl / CHCl₃ / 3 h / 0 °C

3: ethanol / 6 h / Heating

4: H₂ / 10percent Pd/C / methanol / 18 h / 20 °C

5: 3-hydroxybenzotriazole hydrate; 1-[3(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride / dimethylformamide / 4 h / 20 °C

With hydrogenchloride; hydrogen; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; 10percent Pd/C; In methanol; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm000496v

Reference yield:

: 536-25-4
methyl 3-amino-4-hydroxybenzoate

: 1060718-86-6
2-{2-[2-(5-benzyloxycarbonylamino-6-oxo-2-pyridin-4-yl-6H-pyrimidin-1-yl)-acetylamino]-1-hydroxy-3-phenyl-propyl}-benzooxazole-5-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 6 h / Heating

2: H₂ / 10percent Pd/C / methanol / 18 h / 20 °C

3: 3-hydroxybenzotriazole hydrate; 1-[3(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride / dimethylformamide / 4 h / 20 °C

With hydrogen; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 10percent Pd/C; In methanol; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm000496v

Reference yield:

: 66413-45-4
3-(benzyloxycarbonyl)amino-2-hydroxy-4-phenylbutanenitrile

: 1060718-86-6
2-{2-[2-(5-benzyloxycarbonylamino-6-oxo-2-pyridin-4-yl-6H-pyrimidin-1-yl)-acetylamino]-1-hydroxy-3-phenyl-propyl}-benzooxazole-5-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: HCl / CHCl₃ / 3 h / 0 °C

2: ethanol / 6 h / Heating

3: H₂ / 10percent Pd/C / methanol / 18 h / 20 °C

4: 3-hydroxybenzotriazole hydrate; 1-[3(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride / dimethylformamide / 4 h / 20 °C

With hydrogenchloride; hydrogen; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 10percent Pd/C; In methanol; ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm000496v