{(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester

Base Information

Chemical Name:{(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester
CAS No.:1329167-07-8
Molecular Formula:C₂₂H₂₉N₃O₃
Molecular Weight:383.491
Hs Code.:

Synonyms:{(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester

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Chemical Property of {(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester

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Technology Process of {(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester

There total 1 articles about {(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl 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:

: 1329605-36-8
(S)-2-tert-butoxycarbonylamino-pent-4-enoic acid 2-(2-but-3-enyloxyphenyl)-2-oxo ethyl ester

: 1329167-07-8
{(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester

Guidance literature:: With ammonium acetate; In xylene; at 140 ℃; for 0.5h; Microwave irradiation;

Reference yield: 64.0%

: 1329167-07-8
{(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester

: 76513-69-4
(2-trimethylethylsilylethoxy)methyl chloride

: 1329167-08-9
{(S)-1-[4-(2-but-3-enyloxyphenyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester

Guidance literature:: {(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester; With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 1h;

(2-trimethylethylsilylethoxy)methyl chloride; In N,N-dimethyl-formamide; at 0 - 20 ℃;

Reference yield:

: 1329167-07-8
{(S)-1-[4-(2-but-3-enyloxyphenyl)-1H-imidazol-2-yl]but-3-enyl}carbamic acid tert-butyl ester

: 1329159-46-7
(E)-3-(5-chloro-2-tetrazol-1-ylphenyl)-N-(E)-(S)-8-oxa-16,18-diazatricyclo[13.2.1.0(2,7)]octadeca-1⁽¹⁷⁾,2,4,6,11,15⁽¹⁸⁾-hexaen-14-ylacrylamide trifluoroacetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 - 20 °C

1.2: 0 - 20 °C

2.1: toluene-4-sulfonic acid / dichloromethane / 1.5 h / 40 °C / Inert atmosphere

2.2: 1 h

3.1: hydrogenchloride; water / ethanol / 50 °C

3.2: pH 10

4.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.75 h

With hydrogenchloride; water; sodium hydride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; N,N-dimethyl-formamide;