2-(2-Amino-phenyl)-N-methyl-N-((1S,2S)-2-pyrrolidin-1-yl-cyclohexyl)-acetamide; hydrobromide

Base Information

Chemical Name:2-(2-Amino-phenyl)-N-methyl-N-((1S,2S)-2-pyrrolidin-1-yl-cyclohexyl)-acetamide; hydrobromide
CAS No.:118170-31-3
Molecular Formula:BrH*C₁₉H₂₉N₃O
Molecular Weight:396.371
Hs Code.:

Synonyms:2-(2-Amino-phenyl)-N-methyl-N-((1S,2S)-2-pyrrolidin-1-yl-cyclohexyl)-acetamide; hydrobromide

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Chemical Property of 2-(2-Amino-phenyl)-N-methyl-N-((1S,2S)-2-pyrrolidin-1-yl-cyclohexyl)-acetamide; hydrobromide

Chemical Property:

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MSDS Files:: SDS file from LookChem

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Technology Process of 2-(2-Amino-phenyl)-N-methyl-N-((1S,2S)-2-pyrrolidin-1-yl-cyclohexyl)-acetamide; hydrobromide

There total 2 articles about 2-(2-Amino-phenyl)-N-methyl-N-((1S,2S)-2-pyrrolidin-1-yl-cyclohexyl)-acetamide; hydrobromide 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:

: 3740-52-1
2-(2-nitrophenyl)acetic acid

: 118170-31-3
2-(2-Amino-phenyl)-N-methyl-N-((1S,2S)-2-pyrrolidin-1-yl-cyclohexyl)-acetamide; hydrobromide

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / DCC

2: 97 percent / H₂ / 10percent Pd/C / 2585.7 Torr

With hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal;
DOI:10.1021/jm00122a001

Reference yield:

: 67198-53-2
trans-N-methyl-2-(1-pyrrolidinyl)-cyclohexanamine

: 118170-31-3
2-(2-Amino-phenyl)-N-methyl-N-((1S,2S)-2-pyrrolidin-1-yl-cyclohexyl)-acetamide; hydrobromide

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / DCC

2: 97 percent / H₂ / 10percent Pd/C / 2585.7 Torr

With hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal;
DOI:10.1021/jm00122a001