{(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl ester

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Chemical Name:{(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl ester
CAS No.:610796-31-1
Molecular Formula:C₃₀H₃₄N₈O₇S
Molecular Weight:650.715
Hs Code.:

{(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl ester

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Chemical Property of {(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl ester

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Technology Process of {(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl ester

There total 4 articles about {(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl 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:

: 71449-08-6
(2R)-2-{[(benzyloxy)carbonyl]amino}-4-tert-butoxy-4-oxobutanoic acid

: 610796-31-1
{(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: DIPEA / CH₂Cl₂ / -20 °C

2: HBr; AcOH

3: 76 percent / dimethylformamide / 100 °C

4: HATU; DIPEA / dimethylformamide

With hydrogen bromide; acetic acid; 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 dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(03)00578-X

Reference yield:

: 610796-27-5
(R)-3-Benzyloxycarbonylamino-5-bromo-4-oxo-pentanoic acid

: 610796-31-1
{(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / dimethylformamide / 100 °C

2: HATU; DIPEA / dimethylformamide

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;
DOI:10.1016/S0960-894X(03)00578-X

Reference yield:

: 3-benzyloxycarbonylamino-4-isobutoxycarbonyloxy-4-oxo-butyric acid tert-butyl ester

: 610796-31-1
{(R)-1-[2-(2-Benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-2-[methyl-(4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidin-5-yl)-carbamoyl]-ethyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: HBr; AcOH

2: 76 percent / dimethylformamide / 100 °C

3: HATU; DIPEA / dimethylformamide

With hydrogen bromide; acetic acid; 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;
DOI:10.1016/S0960-894X(03)00578-X