(S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester
CAS No.:681425-04-7
Molecular Formula:C₂₂H₂₅F₄N₃O₅
Molecular Weight:487.451
Hs Code.:

(S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

Synonyms:(S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

Suppliers and Price of (S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

There total 12 articles about (S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl 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: 60.0%

: 681425-02-5
(S)-(1α,5α,6α)-3-[4-(5-aminomethyl-2-oxooxazolidin-3-yl)-2,6-difluorophenyl]-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

: 381-73-7
Difluoroacetic acid

: 681425-04-7
(S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

Guidance literature:: With pyridine; diisopropyl-carbodiimide; In N,N-dimethyl-formamide; at 20 ℃; for 16h;
DOI:10.1021/jm058204j

Reference yield:

: 681424-87-3
(1α,5α,6α)-3-benzyloxycarbonyl-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

: 681425-04-7
(S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 9 steps

1.1: 0.423 g / H₂ / Pd(OH)2/C / methanol / 1.5 h

2.1: 92 percent / diisopropylethylamine / dimethylformamide / 20 h / 50 °C

3.1: Fe; aq. NH₄Cl / ethanol / 1.5 h / Heating

4.1: 0.71 g / pyridine / CH₂Cl₂ / 0 - 20 °C

5.1: lithium hexamethyldisilylamide / tetrahydrofuran / 1.5 h / -78 °C

5.2: 87 percent / tetrahydrofuran / 16 h / 20 °C

6.1: 99 percent / Et₃N / CH₂Cl₂ / 0.5 h / 0 °C

7.1: NaN₃ / dimethylformamide / 15 h / 70 °C

8.1: PPh₃ / tetrahydrofuran / 3 h / 20 °C

8.2: 86 percent / H₂O / tetrahydrofuran / 16 h / 40 °C

9.1: 60 percent / pyridine; 1,3-diisopropylcarbodiimide / dimethylformamide / 16 h / 20 °C

With pyridine; sodium azide; hydrogen; iron; ammonium chloride; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium hexamethyldisilazane; diisopropyl-carbodiimide; palladium dihydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm058204j

Reference yield:

: 35059-50-8
t-butyl diazoacetate

: 681425-04-7
(S)-(1α,5α,6α)-3-(4-{5-[(2,2,-difluoroacetylamino)methyl]-2-oxooxazolidin-3-yl}-2,6-difluorophenyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 10 steps

1.1: Rh₂(OAc)4 / CH₂Cl₂

2.1: 0.423 g / H₂ / Pd(OH)2/C / methanol / 1.5 h

3.1: 92 percent / diisopropylethylamine / dimethylformamide / 20 h / 50 °C

4.1: Fe; aq. NH₄Cl / ethanol / 1.5 h / Heating

5.1: 0.71 g / pyridine / CH₂Cl₂ / 0 - 20 °C

6.1: lithium hexamethyldisilylamide / tetrahydrofuran / 1.5 h / -78 °C

6.2: 87 percent / tetrahydrofuran / 16 h / 20 °C

7.1: 99 percent / Et₃N / CH₂Cl₂ / 0.5 h / 0 °C

8.1: NaN₃ / dimethylformamide / 15 h / 70 °C

9.1: PPh₃ / tetrahydrofuran / 3 h / 20 °C

9.2: 86 percent / H₂O / tetrahydrofuran / 16 h / 40 °C

10.1: 60 percent / pyridine; 1,3-diisopropylcarbodiimide / dimethylformamide / 16 h / 20 °C

With pyridine; dirhodium tetraacetate; sodium azide; hydrogen; iron; ammonium chloride; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium hexamethyldisilazane; diisopropyl-carbodiimide; palladium dihydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm058204j