(S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Name:(S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:405115-75-5
Molecular Formula:C₂₄H₃₆N₂O₃
Molecular Weight:400.561
Hs Code.:

Synonyms:(S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of (S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester

There total 6 articles about (S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl 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: 94.0%

: 26250-84-0
(S)-(-)-1-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid

: (1S,2S)-2-Methyl-1-((E)-styryl)-butylamine; hydrochloride

: 405115-75-5
(S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In dichloromethane;
DOI:10.1016/S0960-894X(01)00600-X

Reference yield:

: 13139-16-7
N-(tert-butyloxycarbonyl)-L-isoleucine

: 405115-75-5
(S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / BOP-Cl; Et₃N / CH₂Cl₂

2: 97 percent / LAH / tetrahydrofuran

3: 58 percent / NaN(SiMe₃)2 / tetrahydrofuran

4: 85 percent / HCl / dioxane

5: 94 percent / BOP; Et₃N / CH₂Cl₂

With hydrogenchloride; lithium aluminium tetrahydride; sodium hexamethyldisilazane; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1016/S0960-894X(01)00600-X

Reference yield:

: 1080-32-6
O,O-diethyl benzylphosphonate

: 405115-75-5
(S)-2-[(1S,2S)-2-Methyl-1-((E)-styryl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / NaN(SiMe₃)2 / tetrahydrofuran

2: 85 percent / HCl / dioxane

3: 94 percent / BOP; Et₃N / CH₂Cl₂

With hydrogenchloride; sodium hexamethyldisilazane; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1016/S0960-894X(01)00600-X