allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

Base Information

Chemical Name:allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside
CAS No.:140236-14-2
Molecular Formula:C₄₁H₅₃Cl₆N₂O₁₄P
Molecular Weight:1041.57
Hs Code.:

allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

Synonyms:allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

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Chemical Property of allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

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Technology Process of allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

There total 6 articles about allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside 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: 87.0%

: Dodecanoylamino-acetic acid (2S,3R,4R,5S,6R)-2-allyloxy-5-hydroxy-3-(2,2,2-trichloro-ethoxycarbonylamino)-6-(2,2,2-trichloro-ethoxycarbonyloxymethyl)-tetrahydro-pyran-4-yl ester

: 2524-64-3
chlorophosphoric acid diphenyl ester

: 140236-14-2
allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

Guidance literature:: With pyridine; dmap; for 1h; Ambient temperature;
DOI:10.1248/cpb.39.3244

Reference yield:

: 112-16-3
n-dodecanoyl chloride

: 140236-14-2
allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 88 percent / aq. NaOH / 0.5 h

2: 4-dimethylaminopyridine (DMAP), dicyclohexylcarbodiimide (DCC) / CH₂Cl₂ / 15 h / Ambient temperature

3: 90percent aq. AcOH / 0.33 h / 90 °C

4: 75 percent / pyridine / 1.5 h

5: 87 percent / DMAP, pyridine / 1 h / Ambient temperature

With pyridine; dmap; sodium hydroxide; acetic acid; dicyclohexyl-carbodiimide; In dichloromethane;
DOI:10.1248/cpb.39.3244

Reference yield:

: 7596-88-5
N-dodecanoylglycine

: 140236-14-2
allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 4-dimethylaminopyridine (DMAP), dicyclohexylcarbodiimide (DCC) / CH₂Cl₂ / 15 h / Ambient temperature

2: 90percent aq. AcOH / 0.33 h / 90 °C

3: 75 percent / pyridine / 1.5 h

4: 87 percent / DMAP, pyridine / 1 h / Ambient temperature

With pyridine; dmap; acetic acid; dicyclohexyl-carbodiimide; In dichloromethane;
DOI:10.1248/cpb.39.3244