(1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Base Information

Chemical Name:(1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester
CAS No.:318473-80-2
Molecular Formula:C₂₆H₃₁N₃O₁₀
Molecular Weight:545.546
Hs Code.:

(1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Synonyms:(1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester

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Chemical Property of (1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Chemical Property:

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Technology Process of (1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester

There total 6 articles about (1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl 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: 68.0%

: 250137-94-1
methyl (1S,5S,7R)-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-exo-carboxylate

: 318473-84-6
(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid

: 318473-80-2
(1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In N,N-dimethyl-formamide;
DOI:10.1021/ol006548s

Reference yield:

: 250137-88-3
methyl (1S,5S,7R)-3-benzyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-exo-carboxylate

: 318473-80-2
(1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / H₂ / 20percent Pd(OH)2/C / methanol / 21 h / 760.05 Torr

2: 97 percent / PyBrOP; DIPEA / CH₂Cl₂

3: 100 percent / LiOH / methanol; tetrahydrofuran

4: 68 percent / PyBrOP; DIPEA / dimethylformamide

With lithium hydroxide; hydrogen; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; 20percent Pd(OH)2/C; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 1: Hydrogenolysis / 2: Substitution / 3: Hydrolysis / 4: Substitution;
DOI:10.1021/ol006548s

Reference yield:

: 250137-79-2
(1R,5S,7R)-3-benzyl-2-oxo-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-exo-carboxylic acid methyl ester

: 318473-80-2
(1S,5S,7R)-3-[(1S,5S,7R)-3-((1S,5S,7R)-3-Benzyl-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl)-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carbonyl]-6,8-dioxa-3-aza-bicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: BH₃*Me₂S

2: 100 percent / H₂ / 20percent Pd(OH)2/C / methanol / 21 h / 760.05 Torr

3: 97 percent / PyBrOP; DIPEA / CH₂Cl₂

4: 100 percent / LiOH / methanol; tetrahydrofuran

5: 68 percent / PyBrOP; DIPEA / dimethylformamide

With lithium hydroxide; dimethylsulfide borane complex; hydrogen; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; 20percent Pd(OH)2/C; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 1: Reduction / 2: Hydrogenolysis / 3: Substitution / 4: Hydrolysis / 5: Substitution;
DOI:10.1021/ol006548s