4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester

Base Information

• Chemical Name: 4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester
• CAS No.: 78773-23-6
• Molecular Formula: C₁₆H₁₅F₃N₂O₆
• Molecular Weight: 388.3
• Mol file: 78773-23-6.mol

Synonyms:4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester

Chemical Property of 4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester

There total 3 articles about 4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester 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: 92.0%

(2S,3S,4S)-2-methyl-3-(4-nitrobenzoyloxy)-4-trifluoracetamido-3,4-dihydro-2H-pyran (77398-05-1) + methyl iodide (74-88-4) → 4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester (78773-23-6)

Guidance literature:

With potassium carbonate; In acetone; at 50 ℃;

DOI:10.1021/ja00404a047

Reference yield:

4-nitro-benzoyl chloride (122-04-3) → 4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester (78773-23-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) (dimethylamino)pyridine, pyridine / 1.) room temperature, 2.) 185 deg C, 2.5 torr

2: 92 percent / K₂CO₃ / acetone / 50 °C

With pyridine; dmap; potassium carbonate; In acetone;

DOI:10.1021/ja00404a047

Reference yield:

2,3,6-Trideoxy-3-trifluoroacetamido-L-lixo-hexopyranose (51996-45-3,56354-08-6,64429-67-0,71952-66-4,122350-89-4) → 4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-3,4-dihydro-2H-pyran-3-yl ester (78773-23-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) (dimethylamino)pyridine, pyridine / 1.) room temperature, 2.) 185 deg C, 2.5 torr

2: 92 percent / K₂CO₃ / acetone / 50 °C

With pyridine; dmap; potassium carbonate; In acetone;

DOI:10.1021/ja00404a047

upstream raw materials:

(2S,3S,4S)-2-methyl-3-(4-nitrobenzoyloxy)-4-trifluoracetamido-3,4-dihydro-2H-pyran

methyl iodide

4-nitro-benzoyl chloride

2,3,6-Trideoxy-3-trifluoroacetamido-L-lixo-hexopyranose

Downstream raw materials:

(1S,2S,4R)-2-Ethyl-2,5,7-trihydroxy-4-[(2R,4S,5S,6S)-6-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-5-(4-nitro-benzoyloxy)-tetrahydro-pyran-2-yloxy]-6,11-dioxo-1,2,3,4,6,11-hexahydro-naphthacene-1-carboxylic acid methyl ester

(1R,2R,4S)-2-Ethyl-2,5,7-trihydroxy-4-[(2R,4S,5S,6S)-6-methyl-4-[methyl-(2,2,2-trifluoro-acetyl)-amino]-5-(4-nitro-benzoyloxy)-tetrahydro-pyran-2-yloxy]-6,11-dioxo-1,2,3,4,6,11-hexahydro-naphthacene-1-carboxylic acid methyl ester

aklavin

N-demethylaklavin