N-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine

Base Information

Chemical Name:N-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine
CAS No.:1609396-89-5
Molecular Formula:C₄₀H₃₂FNO₇S
Molecular Weight:689.761
Hs Code.:

Synonyms:N-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine

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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-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine

Chemical Property:

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Technology Process of N-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine

There total 4 articles about N-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine 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: 34.0%

: 6974-32-9
1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose

: 1609396-81-7
7-ethyl-3-fluoro-10H-phenothiazine

: 1609396-89-5
N-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine

Guidance literature:: In toluene; at 155 - 160 ℃; for 10.25h;
DOI:10.1007/s12039-013-0551-2

Reference yield:

: 90382-10-8
2-amino-5-ethylbenzothiazole

: 1609396-89-5
N-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine

Guidance literature:: Multi-step reaction with 4 steps

1: sodium acetate / ethanol / Reflux

2: 4 h / Reflux

3: potassium hydroxide / ethanol; acetone / 4.5 h / Reflux

4: toluene / 10.25 h / 155 - 160 °C

With sodium acetate; potassium hydroxide; In ethanol; acetone; toluene; 3: |Smiles Aromatic Rearrangement;
DOI:10.1007/s12039-013-0551-2

Reference yield:

: 345-17-5
1-chloro-4-fluoro-2-nitrobenzene

: 1609396-89-5
N-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)-7-ethyl-3-fluoro-10H-phenothiazine

Guidance literature:: Multi-step reaction with 4 steps

1: sodium acetate / ethanol / Reflux

2: 4 h / Reflux

3: potassium hydroxide / ethanol; acetone / 4.5 h / Reflux

4: toluene / 10.25 h / 155 - 160 °C

With sodium acetate; potassium hydroxide; In ethanol; acetone; toluene; 3: |Smiles Aromatic Rearrangement;
DOI:10.1007/s12039-013-0551-2