2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

Base Information

Chemical Name:2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide
CAS No.:159780-18-4
Molecular Formula:C₂₈H₃₈F₃N₃O₇Si
Molecular Weight:613.706
Hs Code.:

2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

Synonyms:2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

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Chemical Property of 2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

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Technology Process of 2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

There total 16 articles about 2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide 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:

: 159780-17-3
2-(3-Benzyloxycarbonylamino-4-ethoxycarbonyl-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

: 159780-18-4
2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

Guidance literature:: With lithium hydroxide; In ethanol; at 0 ℃; for 7h;
DOI:10.1021/jm950684z

Reference yield:

: 33707-21-0
dimethyl <3-(dimethylamino)-2-(ethoxycarbonyl)-2-propenylidene>malonate

: 159780-18-4
2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 71 percent / ethanol / 16 h / Heating

2: LiI / pyridine / 14 h / Heating

3: diphenyl phosphorazidate, TEA / dioxane / 4 h / Heating

4: aq. LiOH*H₂O / ethanol / 7 h / 0 °C

With lithium hydroxide; TEA; diphenyl phosphoryl azide; lithium iodide; In 1,4-dioxane; pyridine; ethanol;
DOI:10.1021/jm950684z

Reference yield:

: 106746-09-2
3(RS)-amino-1,1,1-trifluoro-2(RS)-hydroxy-4-methylpentane hydrochloride

: 159780-18-4
2-(3-benzyloxycarbonylamino-4-carboxy-2-oxo-1,2-dihydro-1-pyridyl)-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide

Guidance literature:: Multi-step reaction with 7 steps

1: NMM / tetrahydrofuran / 3 h / 0 °C

2: 62 percent / 2,6-lutidine / CH₂Cl₂ / 3 h / Ambient temperature

3: 96 percent / NaI / acetone / 16 h / Ambient temperature

4: 58 percent / DBU / dimethylformamide / 24 h / Ambient temperature

5: LiI / pyridine / 14 h / Heating

6: diphenyl phosphorazidate, TEA / dioxane / 4 h / Heating

7: aq. LiOH*H₂O / ethanol / 7 h / 0 °C

With 4-methyl-morpholine; 2,6-dimethylpyridine; lithium hydroxide; TEA; diphenyl phosphoryl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium iodide; lithium iodide; In tetrahydrofuran; 1,4-dioxane; pyridine; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm950684z