Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate

Base Information

• Chemical Name: Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate
• CAS No.: 1311385-17-7
• Molecular Formula: C₃₄H₃₅F₂NO₉S
• Molecular Weight: 671.716
• Mol file: 1311385-17-7.mol

Synonyms:Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate

Chemical Property of Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate

There total 4 articles about Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate 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:

bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-hydroxy-bicyclo[3.1.0]hexane-2,6-dicarboxylate (1311385-15-5) + p-toluenesulfonyl chloride (98-59-9) → Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate (1311385-17-7)

Guidance literature:

With dmap; triethylamine; In dichloromethane; at 20 ℃; Inert atmosphere; Cooling with ice;

Reference yield:

bis[(2-fluorophenyl)methyl] (1S,2S,5R,6R)-2-(tert-butoxycarbonylamino)-4-oxo-bicyclo[3.1.0]hexane-2,6-dicarboxylate (1311385-12-2) → Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate (1311385-17-7)

Guidance literature:

Multi-step reaction with 2 steps

1.1: L-Selectride / tetrahydrofuran / 1.75 h / -78 °C / Inert atmosphere

1.2: -78 °C

2.1: dmap; triethylamine / dichloromethane / 20 °C / Inert atmosphere; Cooling with ice

With dmap; L-Selectride; triethylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

(1S,2S,5R,6R)-2-(tert-butoxycarbonylamino)-4-oxo-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid (1311385-14-4) → Bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-(p-tolylsulfonyloxy)bicyclo[3.1.0]hexane-2,6-dicarboxylate (1311385-17-7)

Guidance literature:

Multi-step reaction with 3 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

2.1: L-Selectride / tetrahydrofuran / 1.75 h / -78 °C / Inert atmosphere

2.2: -78 °C

3.1: dmap; triethylamine / dichloromethane / 20 °C / Inert atmosphere; Cooling with ice

With dmap; L-Selectride; caesium carbonate; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

upstream raw materials:

bis[(2-fluorophenyl)methyl] (1S,2S,5R,6R)-2-(tert-butoxycarbonylamino)-4-oxo-bicyclo[3.1.0]hexane-2,6-dicarboxylate

(1S,2S,5R,6R)-2-(tert-butoxycarbonylamino)-4-oxo-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid

bis[(2-fluorophenyl)methyl] (1S,2S,4S,5R,6R)-2-(tert-butoxycarbonylamino)-4-hydroxy-bicyclo[3.1.0]hexane-2,6-dicarboxylate

p-toluenesulfonyl chloride

Downstream raw materials:

bis[(2-fluorophenyl)methyl] (1R,2S,4R,5R,6R)-2-(tert-butoxycarbonylamino)-4-(4H-1,2,4-triazol-3-ylsulfanyl)bicyclo[3.1.0]hexane-2,6-dicarboxylate