(2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:(2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester
CAS No.:675130-52-6
Molecular Formula:C₄₄H₅₃NO₁₄
Molecular Weight:819.903
Hs Code.:

(2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester

Synonyms:(2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester

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Chemical Property of (2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester

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Technology Process of (2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester

There total 8 articles about (2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl 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: 39.0%

: 74808-10-9
O-(2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl)trichloroacetimidate

: 675130-51-5
(2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-hydroxymethyl-piperidine-1-carboxylic acid benzyl ester

: 675130-50-4
(5R,7S,8S,8aR)-7,8-Bis-benzyloxy-5-ethyl-hexahydro-oxazolo[3,4-a]pyridin-3-one

: 675130-52-6
(2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; at -30 ℃; for 2h;
DOI:10.1021/jo035522m

Reference yield:

: 100-39-0
benzyl bromide

: 675130-52-6
(2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / NaH / dimethylformamide / 4.5 h / 20 °C

2: aq. NaOH / methanol / 24 h / 95 °C

3: 712 mg / CH₂Cl₂; H₂O / 4 h / 20 °C

4: 39 percent / BF₃*OEt₂ / CH₂Cl₂ / 2 h / -30 °C

With sodium hydroxide; boron trifluoride diethyl etherate; sodium hydride; In methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jo035522m

Reference yield:

: 675130-42-4,675130-54-8
(5R,8aS)-5-ethyl-4,5,6,8a-tetrahydrooxazolidino[3,4-a]pyridin-3-one

: 675130-52-6
(2R,3S,4S,6R)-3,4-Bis-benzyloxy-6-ethyl-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 86 percent / mCPBA / CH₂Cl₂ / 72 h / 20 °C

2.1: AcOH / 17 h / 100 °C

2.2: 615 mg / K₂CO₃ / methanol; H₂O / 3 h / 20 °C

3.1: 93 percent / NaH / dimethylformamide / 4.5 h / 20 °C

4.1: aq. NaOH / methanol / 24 h / 95 °C

5.1: 712 mg / CH₂Cl₂; H₂O / 4 h / 20 °C

6.1: 39 percent / BF₃*OEt₂ / CH₂Cl₂ / 2 h / -30 °C

With sodium hydroxide; boron trifluoride diethyl etherate; sodium hydride; acetic acid; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jo035522m