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(S)-methyl 3-amino-2-(4-((4-(hydroxymethyl)cyclohexyl)buta-1,3-diynyl)benzamido)-3-methylbutanoate hydrochloride

Base Information Edit
  • Chemical Name:(S)-methyl 3-amino-2-(4-((4-(hydroxymethyl)cyclohexyl)buta-1,3-diynyl)benzamido)-3-methylbutanoate hydrochloride
  • CAS No.:1411941-02-0
  • Molecular Formula:C24H30N2O4*ClH
  • Molecular Weight:446.974
  • Hs Code.:
  • Mol file:1411941-02-0.mol
(S)-methyl 3-amino-2-(4-((4-(hydroxymethyl)cyclohexyl)buta-1,3-diynyl)benzamido)-3-methylbutanoate hydrochloride

Synonyms:(S)-methyl 3-amino-2-(4-((4-(hydroxymethyl)cyclohexyl)buta-1,3-diynyl)benzamido)-3-methylbutanoate hydrochloride

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Chemical Property of (S)-methyl 3-amino-2-(4-((4-(hydroxymethyl)cyclohexyl)buta-1,3-diynyl)benzamido)-3-methylbutanoate hydrochloride Edit
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Technology Process of (S)-methyl 3-amino-2-(4-((4-(hydroxymethyl)cyclohexyl)buta-1,3-diynyl)benzamido)-3-methylbutanoate hydrochloride

There total 10 articles about (S)-methyl 3-amino-2-(4-((4-(hydroxymethyl)cyclohexyl)buta-1,3-diynyl)benzamido)-3-methylbutanoate hydrochloride 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:
Guidance literature:
Multi-step reaction with 7 steps
1.1: sodium hydride / tetrahydrofuran / 3 h / 0 - 15 °C
2.1: triethylamine; oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 - 20 °C
3.1: potassium carbonate; methanol / 15 h / 0 - 20 °C
4.1: N-ethyl-N,N-diisopropylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 20 °C / Inert atmosphere
5.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 20 °C
5.2: pH 4
6.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 5 h / 20 °C
7.1: hydrogenchloride / methanol / 20 °C
With hydrogenchloride; methanol; oxalyl dichloride; lithium hydroxide monohydrate; water; sodium hydride; potassium carbonate; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 9 steps
1.1: hydrogenchloride; thionyl chloride / methanol / 1 h / Cooling with ice; Reflux
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 0 - 20 °C
3.1: sodium hydride / tetrahydrofuran / 3 h / 0 - 15 °C
4.1: triethylamine; oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 - 20 °C
5.1: potassium carbonate; methanol / 15 h / 0 - 20 °C
6.1: N-ethyl-N,N-diisopropylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 20 °C / Inert atmosphere
7.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 20 °C
7.2: pH 4
8.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 5 h / 20 °C
9.1: hydrogenchloride / methanol / 20 °C
With hydrogenchloride; methanol; lithium aluminium tetrahydride; thionyl chloride; oxalyl dichloride; lithium hydroxide monohydrate; water; sodium hydride; potassium carbonate; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
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