6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester

Base Information

Chemical Name:6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester
CAS No.:745050-47-9
Molecular Formula:C₂₉H₄₆N₂O₆S
Molecular Weight:550.76
Hs Code.:

6-[[2-(4-<i>tert</i>-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester

Synonyms:6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester

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Chemical Property of 6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester

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Technology Process of 6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester

There total 4 articles about 6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic 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: 72.0%

: 389140-42-5
methyl 6-[(E)-2-[4-(tert-butoxycarbonylamino)phenyl]ethenylsulfonamido]hexanoate

: 147936-56-9
3-cyclohexyl-1-iodopropane

: 745050-47-9
6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 70 ℃; for 5h;
DOI:10.1021/jm010313k

Reference yield:

: ethyl 4-(tert-butoxycarbonylamino)cyclohexanecarboxylate

: 745050-47-9
6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: 94 percent / diisobutylaluminium hydride / toluene / 2 h / -78 °C

2.1: 94 percent / MnO₂ / CHCl₃ / 12 h / 20 °C

3.1: n-butyl lithium / hexane; tetrahydrofuran / 0.5 h / -78 °C

3.2: 95 percent / hexane; tetrahydrofuran / 1.5 h / -78 - 20 °C

4.1: 86 percent / acetone / 12 h / Heating

5.1: 92 percent / trifephenylphosphine; sulfuryl chloride / CHCl₃ / 2 h / cooling

6.1: 74 percent / triethylamine / CHCl₃ / 0.25 h / cooling

7.1: 72 percent / potassium carbonate / dimethylformamide / 5 h / 70 °C

With manganese(IV) oxide; n-butyllithium; sulfuryl dichloride; diisobutylaluminium hydride; potassium carbonate; triethylamine; triphenylphosphine; In tetrahydrofuran; hexane; chloroform; N,N-dimethyl-formamide; acetone; toluene;
DOI:10.1021/jm010313k

Reference yield:

: 389140-41-4
(E)-2-[4-(tert-butoxycarbonylamino)phenyl]ethenylsulfonyl chloride

: 745050-47-9
6-[[2-(4-tert-butoxycarbonylamino-phenyl)-ethenesulfonyl]-(3-cyclohexyl-propyl)-amino]-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / triethylamine / CHCl₃ / 0.25 h / cooling

2: 72 percent / potassium carbonate / dimethylformamide / 5 h / 70 °C

With potassium carbonate; triethylamine; In chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm010313k