(1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

Base Information

Chemical Name:(1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester
CAS No.:820244-71-1
Molecular Formula:C₂₅H₃₃Cl₂FN₂O₆
Molecular Weight:547.451
Hs Code.:

(1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

Synonyms:(1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

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Chemical Property of (1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

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Technology Process of (1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

There total 7 articles about (1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl 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: 90.0%

: 820244-68-6
(1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-(3,4-dichlorobenzylamino)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

: 74-88-4
methyl iodide

: 820244-71-1
(1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 72h;
DOI:10.1016/j.bmc.2005.12.061

Reference yield:

: 820244-64-2
(1R,2R,3S,5R,6R)-2-(tert-butoxycarbonylamino)-6-fluoro-3-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

: 820244-71-1
(1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 71 percent / pyridine / CH₂Cl₂ / 0 °C

2: 71 percent / sodium azide / dimethylformamide / 30 h / 20 - 30 °C

3: 60 percent / hydrogen / Pd/C / ethanol / 12 h / 20 °C

4: 43 percent / pyridine / CHCl₃ / 19 h / 20 °C

5: 90 percent / K₂CO₃ / dimethylformamide / 72 h / 20 °C

With pyridine; sodium azide; hydrogen; potassium carbonate; palladium on activated charcoal; In ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.12.061

Reference yield:

: 820244-66-4
(1R,2R,3R,5R,6R)-3-azido-2-(tert-butoxycarbonylamino)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

: 820244-71-1
(1R,2R,3R,5R,6R)-2-(tert-butoxycarbonylamino)-3-[(3,4-dichlorobenzyl)(methyl)amino]-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / hydrogen / Pd/C / ethanol / 12 h / 20 °C

2: 43 percent / pyridine / CHCl₃ / 19 h / 20 °C

3: 90 percent / K₂CO₃ / dimethylformamide / 72 h / 20 °C

With pyridine; hydrogen; potassium carbonate; palladium on activated charcoal; In ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.12.061