(1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester

Base Information

• Chemical Name: (1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester
• CAS No.: 137718-71-9
• Molecular Formula: C₂₆H₃₀N₂O₈S
• Molecular Weight: 530.599
• Mol file: 137718-71-9.mol

Synonyms:(1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester

Chemical Property of (1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester

There total 1 articles about (1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl 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:

4-nitrobenzyl chloride (619-73-8) + (1R,4aR,6R,8aS)-6-((1R,5S,7S)-10,10-Dimethyl-3,3-dioxo-3λ6-thia-4-aza-tricyclo[5.2.1.01,5]decane-4-carbonyl)-1-methyl-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridin-3-one (137718-70-8) → (1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester (137718-71-9)

Guidance literature:

With n-butyllithium; Yield given. Multistep reaction; 1.) THF, hexane, -30 deg C, 0.5 h, 2.) THF, hexane, from -30 to -10 deg C, 6 h;

DOI:10.1021/ja00025a035

Reference yield:

(1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester (137718-71-9) → (1R,4aR,6R,8aS)-1-Methyl-3-oxo-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester (137718-75-3)

Guidance literature:

With hydrogen fluoride; In pyridine; for 8h; Ambient temperature;

DOI:10.1021/ja00025a035

Reference yield:

(1R,4aR,6R,8aS)-1-Methyl-3-oxo-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester (137718-71-9) → (1R,4aR,6R,8aS)-7-[2-(1H-Indol-3-yl)-ethyl]-1-methyl-3-oxo-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester (137742-01-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 70percent HF / pyridine; various solvent(s) / 8 h / Ambient temperature

2: NaHCO₃ / acetonitrile / 11 h / 80 °C

With hydrogen fluoride; sodium hydrogencarbonate; In pyridine; acetonitrile;

DOI:10.1021/ja00025a035

upstream raw materials:

4-nitrobenzyl chloride

(1R,4aR,6R,8aS)-6-((1R,5S,7S)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-1-methyl-7-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-pyrano[3,4-c]pyridin-3-one

Downstream raw materials:

(1R,4aR,6R,8aS)-1-Methyl-3-oxo-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester

(1R,4aR,6R,8aS)-7-[2-(1H-Indol-3-yl)-ethyl]-1-methyl-3-oxo-octahydro-pyrano[3,4-c]pyridine-6-carboxylic acid 4-nitro-benzyl ester