{(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester

Base Information

Chemical Name:{(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester
CAS No.:345201-71-0
Molecular Formula:C₂₈H₂₉N₅O₈
Molecular Weight:563.567
Hs Code.:

{(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2<i>H</i>-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester

Synonyms:{(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester

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Chemical Property of {(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester

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Technology Process of {(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester

There total 4 articles about {(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid 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: 72.0%

: 144564-95-4
[N⁴-[(benzyloxy)carbonyl]cytosine-1-yl]acetic acid

: 345201-70-9
(2-allyloxycarbonylamino-benzylamino)-acetic acid methyl ester

: 345201-71-0
{(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jo001650o

Reference yield:

: 5344-90-1
2-Aminobenzyl alcohol

: 345201-71-0
{(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 77 percent / pyridine / CH₂Cl₂ / 1.5 h

2: 58 percent / PPh₃; CBr₄ / tetrahydrofuran / 2 h / 20 °C

3: 92 percent / DIPEA / dimethylformamide / 20 °C

4: 72 percent / HATU; DIPEA / dimethylformamide / 0 - 20 °C

With pyridine; carbon tetrabromide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo001650o

Reference yield:

: 345201-68-5
prop-2-en-1-yl N-[2-(hydroxymethyl)phenyl]carbamate

: 345201-71-0
{(2-allyloxycarbonylamino-benzyl)-[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-amino}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / PPh₃; CBr₄ / tetrahydrofuran / 2 h / 20 °C

2: 92 percent / DIPEA / dimethylformamide / 20 °C

3: 72 percent / HATU; DIPEA / dimethylformamide / 0 - 20 °C

With carbon tetrabromide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jo001650o