2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide

Base Information

Chemical Name:2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide
CAS No.:220903-52-6
Molecular Formula:C₁₆H₂₄N₂O₄
Molecular Weight:308.378
Hs Code.:

Synonyms:2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide

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Chemical Property of 2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide

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Technology Process of 2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide

There total 1 articles about 2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide 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: 77.0%

: 4530-20-5
BOC-glycine

: 30992-29-1
Boc-Aib-OH

: 220903-52-6
2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide

Guidance literature:: With 1-methyl-1H-imidazole; diethyl cyanophosphonate; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm960783s

Reference yield: 84.0%

: 220903-52-6
2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide

: 2-amino-N-(4-methoxyphenyl)-2-methylpropanamide

Guidance literature:: With trifluoroacetic acid; at 20 ℃; for 1h;
DOI:10.1021/jm960783s

Reference yield:

: 220903-52-6
2-<(tert-butyloxycarbonyl)amino>-N-(4-methoxyphenyl)-2-methylpropanamide

: N-(2-hydroxy-ethyl)-4-[1-(4-methoxy-phenylcarbamoyl)-1-methyl-ethylamino]-3,5-dinitro-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / CF₃COOH / 1 h / 20 °C

2: 35 percent / diisopropylethylamine / tetrahydrofuran / 60 h / 20 °C

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1021/jm960783s