di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate

Base Information

Chemical Name:di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate
CAS No.:1377990-41-4
Molecular Formula:C₃₁H₄₂Cl₂N₄O₇S
Molecular Weight:685.669
Hs Code.:

di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate

Synonyms:di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate

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Chemical Property of di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate

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Technology Process of di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate

There total 8 articles about di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]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:

: 1377990-37-8
di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-(1H-1,2,4-triazol-3-ylsulfanyl)bicyclo[3.1.0]hexane-2,6-dicarboxylate

: 74-88-4
methyl iodide

: 1377990-41-4
di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate

Guidance literature:: di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-(1H-1,2,4-triazol-3-ylsulfanyl)bicyclo[3.1.0]hexane-2,6-dicarboxylate; With potassium tert-butylate; In tetrahydrofuran; at -78 ℃; for 0.25h;

methyl iodide; In tetrahydrofuran; at -78 - 20 ℃; for 0.75h;

Reference yield:

: 635318-05-7
(1S,2S,4S,5R,6R)-di-tert-butyl 2-[(tert-butoxycarbonyl)amino]-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylate

: 1377990-41-4
di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: triethylamine / tetrahydrofuran / 0 - 20 °C

2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / Reflux

3.1: water; 4-methyl-morpholine / osmium(VIII) oxide / tert-butyl alcohol; acetone / 5 h / 20 °C

4.1: silver(l) oxide / tetrabutylammomium bromide / N,N-dimethyl-formamide / 20 °C

5.1: triethylamine / tetrahydrofuran / 0 - 20 °C

6.1: potassium carbonate / N,N-dimethyl-formamide / 0.08 h / 20 °C

6.2: 48 h / 85 °C

7.1: potassium tert-butylate / tetrahydrofuran / 0.25 h / -78 °C

7.2: 0.75 h / -78 - 20 °C

With 4-methyl-morpholine; potassium tert-butylate; tetrabutyl ammonium fluoride; water; potassium carbonate; triethylamine; silver(l) oxide; osmium(VIII) oxide; tetrabutylammomium bromide; In tetrahydrofuran; N,N-dimethyl-formamide; acetone; tert-butyl alcohol;

Reference yield:

: 1377990-25-4
di-tert-butyl (1S,2S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-4-[(methylsulfonyl)oxy]bicyclo[3.1.0]hexane-2,6-dicarboxylate

: 1377990-41-4
di-tert-butyl (1R,2R,3S,4S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-[(3,4-dichlorobenzyl)oxy]-4-[(1-methyl-1,2,4-triazol-3-yl)sulfanyl]bicyclo[3.1.0]hexane-2,6-dicarboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / Reflux

2.1: water; 4-methyl-morpholine / osmium(VIII) oxide / tert-butyl alcohol; acetone / 5 h / 20 °C

3.1: silver(l) oxide / tetrabutylammomium bromide / N,N-dimethyl-formamide / 20 °C

4.1: triethylamine / tetrahydrofuran / 0 - 20 °C

5.1: potassium carbonate / N,N-dimethyl-formamide / 0.08 h / 20 °C

5.2: 48 h / 85 °C

6.1: potassium tert-butylate / tetrahydrofuran / 0.25 h / -78 °C

6.2: 0.75 h / -78 - 20 °C

With 4-methyl-morpholine; potassium tert-butylate; tetrabutyl ammonium fluoride; water; potassium carbonate; triethylamine; silver(l) oxide; osmium(VIII) oxide; tetrabutylammomium bromide; In tetrahydrofuran; N,N-dimethyl-formamide; acetone; tert-butyl alcohol;