2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid

Base Information

Chemical Name:2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid
CAS No.:33367-15-6
Molecular Formula:C₁₉H₂₃N₃O₆
Molecular Weight:389.408
Hs Code.:

2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2<i>H</i>-pyrimidin-1-yl)-hexanoic acid

Synonyms:2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid

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Chemical Property of 2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid

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Technology Process of 2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid

There total 5 articles about 2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid 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:

: 316352-66-6
(2S,4S)-3-benzyloxycarbonyl-2-tert-butyl-4-[4-(1-thyminyl)butyl]oxazolidin-5-one

: 33367-15-6
2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; at 0 ℃;
DOI:10.1039/b006843h

Reference yield:

: 4330-20-5
N-3-benzoylthymine

: 33367-15-6
2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: DIAD; Ph₃P

2: 87 percent / NaI / acetone / Heating

3: 25 percent / Bu₃SnCl; AIBN; NaBH₃CN / 2-methyl-propan-2-ol / Heating

4: aq. LiOH / tetrahydrofuran / 0 °C

With lithium hydroxide; 2,2'-azobis(isobutyronitrile); di-isopropyl azodicarboxylate; tributyltin chloride; sodium cyanoborohydride; triphenylphosphine; sodium iodide; In tetrahydrofuran; acetone; tert-butyl alcohol; 1: Alkylation / 2: Substitution / 3: Addition / 4: Hydrolysis;
DOI:10.1039/b006843h

Reference yield:

: 316352-60-0
3-benzoyl-1-(3-bromopropyl)thymine

: 33367-15-6
2-benzyloxycarbonylamino-6-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-hexanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / NaI / acetone / Heating

2: 25 percent / Bu₃SnCl; AIBN; NaBH₃CN / 2-methyl-propan-2-ol / Heating

3: aq. LiOH / tetrahydrofuran / 0 °C

With lithium hydroxide; 2,2'-azobis(isobutyronitrile); tributyltin chloride; sodium cyanoborohydride; sodium iodide; In tetrahydrofuran; acetone; tert-butyl alcohol; 1: Substitution / 2: Addition / 3: Hydrolysis;
DOI:10.1039/b006843h