2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

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Chemical Name:2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside
CAS No.:142270-31-3
Molecular Formula:C₆₀H₆₃ClF₃NO₁₉
Molecular Weight:1194.6
Hs Code.:

2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

Synonyms:2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

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Chemical Property of 2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

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Technology Process of 2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

There total 12 articles about 2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-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: 91.0%

: 142270-30-2
2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-7-O-(tert-butyldimethylsilyl)-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

: 142270-31-3
2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

Guidance literature:: With acetic acid; Ambient temperature;
DOI:10.1016/S0008-6215(00)90553-6

Reference yield:

: 122588-51-6
methyl-2,3,4-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside

: 142270-31-3
2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

Guidance literature:: Multi-step reaction with 10 steps

1: 90 percent / 4-dimethylaminopyridine / pyridine / 2 h / Ambient temperature

2: conc. H₂SO₄ / acetic acid / 0.17 h

3: 78 percent / ZnCl₂ / CH₂Cl₂ / 3 h

4: 1) silver triflate, N-iodosuccinimide, 2) BF₃-etherate / 1) CH₂Cl₂, CH₃CN, 10 min, 2) CH₃CN, 3 h

5: 98 percent / H₂ / 10percent Pd-C / ethyl acetate / 16 h / 3000.2 Torr

6: 4-toluenesulfonic acid / acetonitrile / 0.5 h / Ambient temperature

7: pyridine, 4-dimethylaminopyridine / CH₂Cl₂ / 2 h

8: aq. trifluoracetic acid / acetonitrile / 0.5 h

9: 73 percent / DMTST, molecular sieves 4A / diethyl ether / 2 h / Ambient temperature

10: 91 percent / 70percent aq.AcOH / Ambient temperature

With pyridine; dmap; N-iodo-succinimide; 4 A molecular sieve; sulfuric acid; boron trifluoride diethyl etherate; hydrogen; silver trifluoromethanesulfonate; toluene-4-sulfonic acid; acetic acid; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; trifluoroacetic acid; zinc(II) chloride; palladium on activated charcoal; In pyridine; diethyl ether; dichloromethane; acetic acid; ethyl acetate; acetonitrile;
DOI:10.1016/S0008-6215(00)90553-6

Reference yield:

: 142270-22-2
1,6,7-tri-O-acetyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranose

: 142270-31-3
2-(4-trifluoroacetamidophenyl)ethyl O-<6-O-benzoyl-2,3,4-tri-O-benzyl-L-glycero-α-D-manno-heptopyranosyl>-(1-3)-2,6,7-tri-O-acetyl-4-O-chloroacetyl-L-glycero-α-D-manno-heptopyranoside

Guidance literature:: Multi-step reaction with 8 steps

1: 78 percent / ZnCl₂ / CH₂Cl₂ / 3 h

2: 1) silver triflate, N-iodosuccinimide, 2) BF₃-etherate / 1) CH₂Cl₂, CH₃CN, 10 min, 2) CH₃CN, 3 h

3: 98 percent / H₂ / 10percent Pd-C / ethyl acetate / 16 h / 3000.2 Torr

4: 4-toluenesulfonic acid / acetonitrile / 0.5 h / Ambient temperature

5: pyridine, 4-dimethylaminopyridine / CH₂Cl₂ / 2 h

6: aq. trifluoracetic acid / acetonitrile / 0.5 h

7: 73 percent / DMTST, molecular sieves 4A / diethyl ether / 2 h / Ambient temperature

8: 91 percent / 70percent aq.AcOH / Ambient temperature

With pyridine; dmap; N-iodo-succinimide; 4 A molecular sieve; boron trifluoride diethyl etherate; hydrogen; silver trifluoromethanesulfonate; toluene-4-sulfonic acid; acetic acid; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; trifluoroacetic acid; zinc(II) chloride; palladium on activated charcoal; In diethyl ether; dichloromethane; ethyl acetate; acetonitrile;
DOI:10.1016/S0008-6215(00)90553-6