(1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

Base Information

Chemical Name:(1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane
CAS No.:1019853-17-8
Molecular Formula:C₁₃H₁₇NO₃S
Molecular Weight:267.349
Hs Code.:

Synonyms:(1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

Suppliers and Price of (1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

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 (1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

There total 5 articles about (1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane 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: 87.0%

: 1019853-14-5
(R)-4-methyl-N-(1-methyl-2-oxo-propyl)-benzenesulfonamide

: diphenyl(vinyl)sulfonium trifluoromethanesulfonate

: 1(R),2(R),5(S)-1,2-dimethyl-3-(toluene-4-sulfonyl)-6-oxa-3-aza-bicyclo[3.1.0]hexane

: 1019853-17-8
(1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 ℃; optical yield given as %de; Inert atmosphere;
DOI:10.1021/ol800318h

Reference yield: 80.0%

: 3-(7,7-dimethyl-2-oxo-bicyclo[2.2.1]hept-1-yl)-2-vinyl-2-thionia-bicyclo[2.2.1]heptane trifluoromethanesulfonate

: 1019853-14-5
(R)-4-methyl-N-(1-methyl-2-oxo-propyl)-benzenesulfonamide

: 1019853-17-8
(1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

Guidance literature:: With sodium hydride; In dichloromethane; at 0 ℃; Inert atmosphere;
DOI:10.1021/ol800318h

Reference yield:

: 1019853-14-5
(R)-4-methyl-N-(1-methyl-2-oxo-propyl)-benzenesulfonamide

: (1S,2S,5R)-6-(2-bromoethyl)-4,7,7-trimethyl-6-thiabicyclo[3.2.1]octan-6-ium trifluoromethanesulfonate

: 1019853-17-8
(1S,2R,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

: (1S,2S,5R)-1,2-dimethyl-3-[(4-methylphenyl)sulfonyl]-6-oxa-3-azabicyclo[3.1.0]hexane

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 ℃; Overall yield = 60 %; diastereoselective reaction;
DOI:10.1002/hlca.201200455