{(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester
CAS No.:154611-90-2
Molecular Formula:C₃₁H₄₇N₅O₄S
Molecular Weight:585.811
Hs Code.:

{(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

Synonyms:{(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

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Chemical Property of {(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

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Technology Process of {(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

There total 8 articles about {(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic 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:

: 98760-08-8,98818-34-9,98818-35-0,103127-56-6,98737-29-2
(1-oxiranyl-2-phenylethyl)carbamic acid tert-butyl ester

: 154612-97-2
(2S,4R)-4-(2,6-Dimethyl-pyrimidin-4-ylsulfanyl)-piperidine-2-carboxylic acid tert-butylamide

: 154611-90-2
{(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

Guidance literature:: With lithium chloride; In ethanol; at 60 ℃; for 22h;
DOI:10.1021/jm990336n

Reference yield:

: 4472-45-1
4-chloro-2,6-dimethylpyrimidine

: 154611-90-2
{(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / NaH / dimethylformamide / 1 h / 0 °C

2: 4N HCl in dioxane / 0.33 h / 20 °C

3: LiCl / ethanol / 22 h / 60 °C

With hydrogenchloride; sodium hydride; lithium chloride; In ethanol; N,N-dimethyl-formamide; 1: Condensation / 2: acidolysis / 3: Addition;
DOI:10.1021/jm990336n

Reference yield:

: 175671-47-3
(2S,4R)-4-hydroxypipecolic tert-butylamide

: 154611-90-2
{(1S,2R)-1-Benzyl-3-[(2S,4R)-2-tert-butylcarbamoyl-4-(2,6-dimethyl-pyrimidin-4-ylsulfanyl)-piperidin-1-yl]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: Et₃N / tetrahydrofuran / 2 h / 20 °C

2: nBu₄NI / tetrahydrofuran / 15 h / Heating

3: 68 percent / dimethylformamide / 2 h / 45 °C

4: 1N aq. NaOH / methanol; tetrahydrofuran / 1.5 h / 0 °C

5: 73 percent / NaH / dimethylformamide / 1 h / 0 °C

6: 4N HCl in dioxane / 0.33 h / 20 °C

7: LiCl / ethanol / 22 h / 60 °C

With hydrogenchloride; sodium hydroxide; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; lithium chloride; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; 1: mesylation / 2: Iodination / 3: Substitution / 4: Hydrolysis / 5: Condensation / 6: acidolysis / 7: Addition;
DOI:10.1021/jm990336n