(1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester

Base Information

Chemical Name:(1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester
CAS No.:153430-94-5
Molecular Formula:C₄₃H₆₃N₃O₁₂
Molecular Weight:813.986
Hs Code.:

(1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester

Synonyms:(1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester

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Chemical Property of (1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester

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Technology Process of (1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester

There total 7 articles about (1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-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: 91.0%

: 153430-93-4
C₄₉H₇₇N₃O₁₂Si

: 153430-94-5
(1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; for 1.16667h; Ambient temperature;
DOI:10.1021/jm950893j

Reference yield:

: 138682-84-5,144786-97-0,146075-86-7,148152-80-1,149656-40-6,142561-96-4
zaragozic acid A

: 153430-94-5
(1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 1.) conc. hydrochloric acid / 1.) methanol, RT, 24 h, 2.) toluene, 80 deg C, 3.25 h

2: 76 percent / imidazole / dimethylformamide / 16.5 h / 65 °C

3: 98 percent / 0.1 M sodium hydroxide / tetrahydrofuran / 0.5 h / Ambient temperature

4: 1.) N-hydroxysuccinimide, N,N-dicyclohexylcarbodiimide, 2.) sodium borohydride / 1.) THF, RT, 17 h, 2.) DMF, RT, 55 min

5: 95 percent / 2,4,6-collidine / CH₂Cl₂ / 0.75 h

6: 91 percent / sodium azide / dimethylformamide / 4 h / 20 °C

7: 91 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1.17 h / Ambient temperature

With 1H-imidazole; 2,4,6-trimethyl-pyridine; hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; 1-hydroxy-pyrrolidine-2,5-dione; sodium azide; tetrabutyl ammonium fluoride; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm950893j

Reference yield:

: 144571-48-2
(1S,3S,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-3,4,5-tricarboxylic acid 4,5-di-tert-butyl ester 3-methyl ester

: 153430-94-5
(1S,3R,4S,5R,6R,7R)-1-((4S,5R)-4-Acetoxy-5-methyl-3-methylene-6-phenyl-hexyl)-3-azidomethyl-6-((E)-(4S,6S)-4,6-dimethyl-oct-2-enoyloxy)-4,7-dihydroxy-2,8-dioxa-bicyclo[3.2.1]octane-4,5-dicarboxylic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 76 percent / imidazole / dimethylformamide / 16.5 h / 65 °C

2: 98 percent / 0.1 M sodium hydroxide / tetrahydrofuran / 0.5 h / Ambient temperature

3: 1.) N-hydroxysuccinimide, N,N-dicyclohexylcarbodiimide, 2.) sodium borohydride / 1.) THF, RT, 17 h, 2.) DMF, RT, 55 min

4: 95 percent / 2,4,6-collidine / CH₂Cl₂ / 0.75 h

5: 91 percent / sodium azide / dimethylformamide / 4 h / 20 °C

6: 91 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1.17 h / Ambient temperature

With 1H-imidazole; 2,4,6-trimethyl-pyridine; sodium hydroxide; sodium tetrahydroborate; 1-hydroxy-pyrrolidine-2,5-dione; sodium azide; tetrabutyl ammonium fluoride; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm950893j