2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester

Base Information

Chemical Name:2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester
CAS No.:358365-66-9
Molecular Formula:C₂₇H₃₈N₂O₆
Molecular Weight:486.609
Hs Code.:

2-[2-(2-<i>tert</i>-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester

Synonyms:2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester

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Chemical Property of 2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester

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Technology Process of 2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester

There total 14 articles about 2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric 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: 74.0%

: 131423-64-8
benzyl (R)-4-methyl-2-(trifluoromethylsulfonyloxy)pentanoate

: 358365-65-8
[2-(2-amino-6-methoxy-phenyl)-1-hydroxymethyl-ethyl]-carbamic acid tert-butyl ester

: 358365-66-9
2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester

Guidance literature:: With 2,6-dimethylpyridine; In 1,2-dichloro-ethane;
DOI:10.1016/S0040-4039(01)00747-X

Reference yield:

: 554-84-7
meta-nitrophenol

: 358365-66-9
2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 98 percent / K₂CO₃ / acetone / Heating

2.1: 1,2-dichloro-benzene / 6 h / 150 °C

3.1: 87 percent / K₂CO₃ / acetone

4.1: Hg(NO₃)2 / CH₂Cl₂ / 24 h / Heating

4.2: aq. NaCl / 3 h / 20 °C

4.3: NaBH₄; O₂ / dimethylformamide

5.1: 85 percent / H₂ / Pd/C / ethanol

6.1: 74 percent / 2,6-lutidine / 1,2-dichloro-ethane

With 2,6-dimethylpyridine; hydrogen; potassium carbonate; mercury(II) nitrate; palladium on activated charcoal; In ethanol; dichloromethane; 1,2-dichloro-ethane; 1,2-dichloro-benzene; acetone; 2.1: Claisen rearrangement;
DOI:10.1016/S0040-4039(01)00747-X

Reference yield:

: 58621-42-4
2-allyl-1-hydroxy-3-nitrobenzene

: 358365-66-9
2-[2-(2-tert-butoxycarbonylamino-3-hydroxy-propyl)-3-methoxy-phenylamino]-3-methyl-butyric acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 87 percent / K₂CO₃ / acetone

2.1: Hg(NO₃)2 / CH₂Cl₂ / 24 h / Heating

2.2: aq. NaCl / 3 h / 20 °C

2.3: NaBH₄; O₂ / dimethylformamide

3.1: 85 percent / H₂ / Pd/C / ethanol

4.1: 74 percent / 2,6-lutidine / 1,2-dichloro-ethane

With 2,6-dimethylpyridine; hydrogen; potassium carbonate; mercury(II) nitrate; palladium on activated charcoal; In ethanol; dichloromethane; 1,2-dichloro-ethane; acetone;
DOI:10.1016/S0040-4039(01)00747-X