3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol

Base Information

Chemical Name:3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol
CAS No.:171007-26-4
Molecular Formula:C₃₂H₃₈N₂O₂
Molecular Weight:482.666
Hs Code.:

Synonyms:3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol

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Chemical Property of 3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol

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Technology Process of 3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol

There total 4 articles about 3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol 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: 85.0%

: 7065-46-5
3,3-dimethylbutanoic acid chloride

: 171007-18-4
3-(3'-indolyl)-(2S)-(N-methylamino)-1,1-di(4''-methylphenyl)-1-propanol

: 171007-26-4
3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 17h;
DOI:10.1016/S0957-4166(00)00189-0

Reference yield:

: 526-31-8
L-abrine

: 171007-26-4
3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / SOCl₂ / 48 h / 20 °C

2: 59 percent / tetrahydrofuran / 15 h / 20 °C

3: 85 percent / Et₃N / tetrahydrofuran / 17 h / 20 °C

With thionyl chloride; triethylamine; In tetrahydrofuran; 1: Esterification / 2: Addition / 3: Acylation;
DOI:10.1016/S0957-4166(00)00189-0

Reference yield:

: 32164-04-8
(S)-(+)-N_b-methyltryptophan methyl ester

: 171007-26-4
3-(3'-indolyl)-(2S)-(N-methyl-N-3'',3''-dimethylbutyrylamino)-1,1-di(4'''-methylphenyl)-1-propanol

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / tetrahydrofuran / 15 h / 20 °C

2: 85 percent / Et₃N / tetrahydrofuran / 17 h / 20 °C

With triethylamine; In tetrahydrofuran; 1: Addition / 2: Acylation;
DOI:10.1016/S0957-4166(00)00189-0