[[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic acid methyl ester

Base Information

Chemical Name:[[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic acid methyl ester
CAS No.:1313365-98-8
Molecular Formula:C₂₅H₄₀IN₃O₄
Molecular Weight:573.515
Hs Code.:

Synonyms:[[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic acid methyl ester

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Chemical Property of [[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic acid methyl ester

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Technology Process of [[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic acid methyl ester

There total 9 articles about [[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic 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: 90.0%

: 1313365-94-4
(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexylamino)-acetic acid methyl ester

: 123387-72-4
O-tert-butyl N-methyl-N-(2-oxoethyl)carbamate

: 1313365-98-8
[[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic acid methyl ester

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane; at 0 - 20 ℃; for 1h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.5b00810

Reference yield:

: 540-37-4
p-aminoiodobenzene

: 1313365-98-8
[[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 1 h / 20 °C

2.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane; water / 2 h / 20 °C

3.1: trifluoroacetic acid / dichloromethane / 0 - 20 °C

3.2: 0 °C / pH 9

4.1: potassium carbonate / N,N-dimethyl-formamide / 4.5 h / -10 - 10 °C

5.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 0 - 20 °C

5.2: pH 8

With sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; trifluoroacetic acid; In dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1313365-58-0
{4-[(4-iodo-phenylamino)-methyl]-trans-cyclohexyl}-carbamic acid tert-butyl ester

: 1313365-98-8
[[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-(4-{[(4-iodo-phenyl)-methyl-amino]-methyl}-trans-cyclohexyl)-amino]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane; water / 2 h / 20 °C

2.1: trifluoroacetic acid / dichloromethane / 0 - 20 °C

2.2: 0 °C / pH 9

3.1: potassium carbonate / N,N-dimethyl-formamide / 4.5 h / -10 - 10 °C

4.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 0 - 20 °C

4.2: pH 8

With sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; trifluoroacetic acid; In dichloromethane; water; N,N-dimethyl-formamide;