N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, methyl ester

Base Information

Chemical Name:N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, methyl ester
CAS No.:109013-59-4
Molecular Formula:C₂₁H₂₉N₃O₆
Molecular Weight:419.478
Hs Code.:

Synonyms:N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, methyl ester

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Chemical Property of N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, methyl ester

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Technology Process of N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, methyl ester

There total 5 articles about N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, 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:

: 109013-69-6
5-((S)-2-tert-Butoxycarbonylamino-2-methoxycarbonyl-ethyl)-1-(3,4-dimethoxy-benzyl)-3-(2-oxo-2-phenyl-ethyl)-3H-imidazol-1-ium; chloride

: 109013-59-4
N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, methyl ester

Guidance literature:: With acetic acid; zinc; In methanol; for 7h; Yield given; Ambient temperature;
DOI:10.1021/jo00392a018

Reference yield:

: 69614-04-6
S-(+)-7-Methoxycarbonyl-5,6,7,8-tetrahydroimidazo<1,5-c>pyrimidin-5-on

: 109013-59-4
N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / acetonitrile / 6 h / Heating

2: 85 percent / diisopropylethylamine / 120 h / Heating

3: 2.7 g / acetonitrile / 24 h / Heating

4: Zn, acetic acid / methanol / 7 h / Ambient temperature

With acetic acid; N-ethyl-N,N-diisopropylamine; zinc; In methanol; acetonitrile;
DOI:10.1021/jo00392a018

Reference yield:

: 109013-66-3
(S)-5,6,7,8-tetrahydro-7-(methoxycarbonyl)-2-(2'-oxo-2'-phenylethyl)-5-oxoimidazo<1,5-c>pyrimidinium bromide

: 109013-59-4
N-(tert-butoxycarbonyl)-3-<(3,4-dimethoxyphenyl)methyl>-L-histidine, methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / diisopropylethylamine / 120 h / Heating

2: 2.7 g / acetonitrile / 24 h / Heating

3: Zn, acetic acid / methanol / 7 h / Ambient temperature

With acetic acid; N-ethyl-N,N-diisopropylamine; zinc; In methanol; acetonitrile;
DOI:10.1021/jo00392a018