(2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Base Information

Chemical Name:(2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester
CAS No.:183239-81-8
Molecular Formula:C₂₂H₂₂Cl₆N₂O₁₀
Molecular Weight:687.142
Hs Code.:

(2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Synonyms:(2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

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Chemical Property of (2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

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Technology Process of (2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

There total 1 articles about (2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-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: 74.0%

: 545-06-2
trichloroacetonitrile

: (2S,4aR,7R,8R,8aS)-8-Benzoyloxy-6-hydroxy-2-methyl-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

: 183239-81-8
(2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Guidance literature:: With potassium carbonate; In dichloromethane; for 48h; Ambient temperature;
DOI:10.1002/jlac.199619961016

Reference yield: 97.0%

: 61236-87-1
allyl 2,4,6-tri-O-benzyl-α-D-galactopyranoside

: 183239-81-8
(2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

: 183239-82-9
(2S,4aR,6S,7R,8R,8aS)-6-((2S,3R,4S,5S,6R)-2-Allyloxy-3,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-yloxy)-8-benzoyloxy-2-methyl-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; In dichloromethane; 1.) r.t., 1 h, 2.) -23 deg C, 2 h;
DOI:10.1002/jlac.199619961016

Reference yield:

: 183239-81-8
(2S,4aR,6R,7R,8R,8aS)-8-Benzoyloxy-2-methyl-6-(2,2,2-trichloro-acetimidoyloxy)-7-(2,2,2-trichloro-ethoxycarbonylamino)-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

: (2S,4aR,6S,7R,8R,8aS)-7-Acetylamino-8-benzoyloxy-6-[(2R,3S,4S,5R,6S)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-(2-oxo-propoxy)-tetrahydro-pyran-4-yloxy]-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / molecular sieves 4 Angstroem, TMSOTf / CH₂Cl₂ / 1.) r.t., 1 h, 2.) -23 deg C, 2 h

2: Zn, AcOH / 1 h / Ambient temperature

3: pyridine / 0 °C

4: 23 percent / 90percent aq. AcOH / PdCl₂ / 4 h / 60 °C

With pyridine; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; acetic acid; zinc; palladium dichloride; In dichloromethane;
DOI:10.1002/jlac.199619961016