N-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea

Base Information

Chemical Name:N-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea
CAS No.:1171112-63-2
Molecular Formula:C₂₂H₂₅ClN₂O₁₁
Molecular Weight:528.9
Hs Code.:

Synonyms:N-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea

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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-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea

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Technology Process of N-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea

There total 3 articles about N-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea 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: 67.0%

: 4461-36-3
4-chlorobenzoyl isocyanate

: 41355-50-4,51642-81-0,58484-22-3,70128-27-7,70145-20-9,94482-21-0,98300-76-6
2,3,4,6-tetra-O-acetyl-D-glucosyl-1-amine

: 1171112-63-2
N-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea

Guidance literature:: In acetonitrile; at 20 ℃;
DOI:10.1016/j.carres.2008.01.045

Reference yield:

: 122-01-0
4-chloro-benzoyl chloride

: 1171112-63-2
N-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea

Guidance literature:: Multi-step reaction with 2 steps

1: tin(IV) chloride / acetonitrile / 8 h / Reflux; Inert atmosphere

2: acetonitrile / 0.5 h / 20 °C / Inert atmosphere

With tin(IV) chloride; In acetonitrile;
DOI:10.1016/j.bmc.2011.12.059

Reference yield:

: 619-56-7
4-chlorobenzamide

: 1171112-63-2
N-(4-chlorobenzoyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)urea

Guidance literature:: Multi-step reaction with 2 steps

1: 1,2-dichloro-ethane / 24 h / Reflux

2: acetonitrile / 0.5 h / 20 °C / Inert atmosphere

In 1,2-dichloro-ethane; acetonitrile;
DOI:10.1016/j.bmc.2011.12.059