Carbamic acid, [(1S)-1-[1-hydroxy-2-oxo-2-[[(1R)-1-phenylethyl]amino]ethyl]pentyl]-, [1-[[[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy]methyl]cyclobutyl]methyl ester

Base Information

Chemical Name:Carbamic acid, [(1S)-1-[1-hydroxy-2-oxo-2-[[(1R)-1-phenylethyl]amino]ethyl]pentyl]-, [1-[[[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy]methyl]cyclobutyl]methyl ester
CAS No.:568591-63-9
Molecular Formula:C36H48N6O5
Molecular Weight:644.814
Hs Code.:

Carbamic acid,
[(1S)-1-[1-hydroxy-2-oxo-2-[[(1R)-1-phenylethyl]amino]ethyl]pentyl]-,
[1-[[[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy]methyl]cyclobutyl]methyl
ester

Synonyms:

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Chemical Property of Carbamic acid, [(1S)-1-[1-hydroxy-2-oxo-2-[[(1R)-1-phenylethyl]amino]ethyl]pentyl]-, [1-[[[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy]methyl]cyclobutyl]methyl ester

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Technology Process of Carbamic acid, [(1S)-1-[1-hydroxy-2-oxo-2-[[(1R)-1-phenylethyl]amino]ethyl]pentyl]-, [1-[[[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy]methyl]cyclobutyl]methyl ester

There total 6 articles about Carbamic acid, [(1S)-1-[1-hydroxy-2-oxo-2-[[(1R)-1-phenylethyl]amino]ethyl]pentyl]-, [1-[[[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy]methyl]cyclobutyl]methyl 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:

: 497946-74-4
(3S)-3-amino-2-hydroxy-N-[(1R)-1-phenylethyl]heptanamide

: C₂₁H₂₅ClN₄O₃

: 568591-63-9
[1-({[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy}methyl)cyclobutyl]methyl (1S)-1-(1-hydroxy-2-oxo-2-{[(1R)-1-phenylethyl]amino}ethyl)pentylcarbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 0 ℃; for 6h;
DOI:10.1021/jm040107n

Reference yield:

: 4415-73-0
[1-(hydroxymethyl)cyclobutyl]methanol

: 568591-63-9
[1-({[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy}methyl)cyclobutyl]methyl (1S)-1-(1-hydroxy-2-oxo-2-{[(1R)-1-phenylethyl]amino}ethyl)pentylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaH / tetrahydrofuran; dimethylformamide / 0.25 h / 20 °C

1.2: tetrahydrofuran; dimethylformamide / 2 h / 20 °C

2.1: dimethylformamide / 3 h / 90 °C

3.1: CH₂Cl₂; toluene / 16 h / 0 °C

4.1: N,N-diisopropylethylamine / tetrahydrofuran / 6 h / 0 °C

With sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm040107n

Reference yield:

: 3779-29-1
diethyl cyclobutane-1,1-dicarboxylate

: 568591-63-9
[1-({[2-(4-phenyl-1-piperazinyl)-4-pyrimidinyl]oxy}methyl)cyclobutyl]methyl (1S)-1-(1-hydroxy-2-oxo-2-{[(1R)-1-phenylethyl]amino}ethyl)pentylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 95 percent / lithium aluminum hydride / diethyl ether; tetrahydrofuran / 3 h / 20 °C

2.1: NaH / tetrahydrofuran; dimethylformamide / 0.25 h / 20 °C

2.2: tetrahydrofuran; dimethylformamide / 2 h / 20 °C

3.1: dimethylformamide / 3 h / 90 °C

4.1: CH₂Cl₂; toluene / 16 h / 0 °C

5.1: N,N-diisopropylethylamine / tetrahydrofuran / 6 h / 0 °C

With lithium aluminium tetrahydride; sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm040107n