2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside

Base Information

Chemical Name:2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside
CAS No.:286845-69-0
Molecular Formula:C₄₂H₄₆F₃NO₉
Molecular Weight:765.824
Hs Code.:

Synonyms:2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside

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Chemical Property of 2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside

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Technology Process of 2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside

There total 9 articles about 2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside 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: 60.0%

: 140231-91-0
Ethyl 6,7-O-di-O-benzyl-2,3-O-isopropylidene-4-O-(4-methoxy)benzyl-1-thio-L-glycero-α-D-manno-heptopyranoside

: 115166-92-2
2-[4-(trifluoroacetylamino)phenyl]ethanol

: 2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-β-D-manno-heptopyranoside

: 286845-69-0
2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside

Guidance literature:: With N-iodo-succinimide; 4 A molecular sieve; silver trifluoromethanesulfonate; In dichloromethane; acetonitrile; at 20 ℃; for 1.5h;
DOI:10.1016/S0957-4166(99)00554-6

Reference yield:

: 7473-36-1,13533-58-9,36400-88-1,56245-60-4,73494-52-7,73804-33-8,128946-17-8,686299-00-3
ethyl 1-thio-α-D-mannopyranoside

: 286845-69-0
2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside

Guidance literature:: Multi-step reaction with 8 steps

1.1: pyridine; 4-dimethylaminopyridine

2.1: p-toluenesulfonic acid / dimethylformamide / 2 h / 20 °C

3.1: NaH / dimethylformamide / 1 h / 0 °C

3.2: 80 percent / dimethylformamide / 2 h / 0 °C

4.1: 62 percent / aq. formic acid / ethyl acetate / 2.5 h

5.1: oxalyl chloride; DMSO / CH₂Cl₂ / 0.5 h / -60 °C

6.1: 31 percent / Mg; HgBr₂ / tetrahydrofuran / 10 - 20 °C

7.1: NaH / light petroleum; dimethylformamide / 2 h

7.2: 82 percent / light petroleum; dimethylformamide / 2 h / 20 °C

8.1: 60 percent / molecular sieves 4A; NIS; AgOTf / CH₂Cl₂; acetonitrile / 1.5 h / 20 °C

With pyridine; dmap; N-iodo-succinimide; formic acid; oxalyl dichloride; 4 A molecular sieve; silver trifluoromethanesulfonate; sodium hydride; toluene-4-sulfonic acid; magnesium; dimethyl sulfoxide; mercury dibromide; In tetrahydrofuran; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; Petroleum ether; 1.1: Alkylation / 2.1: acetalization / 3.1: Metallation / 3.2: Substitution / 4.1: Hydrolysis / 5.1: Oxidation / 6.1: Grignard reaction / 7.1: Metallation / 7.2: Substitution / 8.1: Substitution;
DOI:10.1016/S0957-4166(99)00554-6

Reference yield:

: 128850-48-6
ethyl 1-thio-6-O-triphenylmethyl-α-D-mannopyranoside

: 286845-69-0
2-(4-trifluoroacetamidophenyl)ethyl 6,7-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-L-glycero-α-D-manno-heptopyranoside

Guidance literature:: Multi-step reaction with 7 steps

1.1: p-toluenesulfonic acid / dimethylformamide / 2 h / 20 °C

2.1: NaH / dimethylformamide / 1 h / 0 °C

2.2: 80 percent / dimethylformamide / 2 h / 0 °C

3.1: 62 percent / aq. formic acid / ethyl acetate / 2.5 h

4.1: oxalyl chloride; DMSO / CH₂Cl₂ / 0.5 h / -60 °C

5.1: 31 percent / Mg; HgBr₂ / tetrahydrofuran / 10 - 20 °C

6.1: NaH / light petroleum; dimethylformamide / 2 h

6.2: 82 percent / light petroleum; dimethylformamide / 2 h / 20 °C

7.1: 60 percent / molecular sieves 4A; NIS; AgOTf / CH₂Cl₂; acetonitrile / 1.5 h / 20 °C

With N-iodo-succinimide; formic acid; oxalyl dichloride; 4 A molecular sieve; silver trifluoromethanesulfonate; sodium hydride; toluene-4-sulfonic acid; magnesium; dimethyl sulfoxide; mercury dibromide; In tetrahydrofuran; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; Petroleum ether; 1.1: acetalization / 2.1: Metallation / 2.2: Substitution / 3.1: Hydrolysis / 4.1: Oxidation / 5.1: Grignard reaction / 6.1: Metallation / 6.2: Substitution / 7.1: Substitution;
DOI:10.1016/S0957-4166(99)00554-6