N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside

Base Information

Chemical Name:N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside
CAS No.:1206451-74-2
Molecular Formula:C₅₀H₅₃NO₁₃
Molecular Weight:875.97
Hs Code.:

Synonyms:N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside

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Technology Process of N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside

There total 1 articles about N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside 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: 80.0%

: N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-3-O-chloroacetyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside

: 1206451-74-2
N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydrogencarbonate; thiourea; In tetrahydrofuran; at 55 ℃; for 12h;
DOI:10.1039/b914534f

Reference yield:

: 1206451-93-5
4-azido-2,3,6-tri-O-benzoyl-4-deoxy-α-D-glucopyranosyl trichloroacetimidate

: 1206451-74-2
N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside

: 1206451-97-9
N-benzyloxycarbonylaminoethyl 4-azido-2,3,6-tri-O-benzoyl-4-deoxy-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -50 ℃; for 1h; Inert atmosphere; Molecular sieve;
DOI:10.1039/b914534f

Reference yield:

: 1206451-76-4
2-O-acetyl-4-azido-3-O-benzoyl-4,6-dideoxy-D-glucopyranosyl trichloroacetimidate

: 1206451-74-2
N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside

: 1206451-77-5
N-benzyloxycarbonylaminoethyl 2-O-benzoyl-4-azido-3-O-benzoyl-4,6-dideoxy-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -70 ℃; for 0.75h; Molecular sieve; Inert atmosphere;
DOI:10.1039/b914534f