6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid

Base Information

Chemical Name:6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid
CAS No.:108998-85-2
Molecular Formula:C₂₃H₂₂N₆O₈S₂
Molecular Weight:574.595
Hs Code.:

6-<<N-<(S)-2-carbamoyl-2-<(o-nitrophenylthio)amino>ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid

Synonyms:6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid

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Chemical Property of 6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid

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Technology Process of 6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid

There total 6 articles about 6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid 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: 62.0%

: 109880-42-4
methyl 6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylate

: 108998-85-2
6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; 0 deg C, then RT, 3 h;
DOI:10.1016/S0040-4020(88)90018-X

Reference yield:

: 19872-93-6
dimethyl 4-methoxypyridine-2,6-dicarboxylate

: 108998-85-2
6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 85 percent / NaBH₄ / methanol / 0 deg C to RT, 3 h

2: 1.) (COCl)2, 2.) Et₃N / 1.) DMSO, CH₂Cl₂, -30 deg C, 20 min, 2.) -60 deg C, 25 min, then RT

3: 89 percent

4: 86 percent / trifluoroacetic acid, Et₃N / CH₂Cl₂ / 0 deg C, 30 min, then RT, 6 h

5: 62 percent / LiOH / tetrahydrofuran / 0 deg C, then RT, 3 h

With lithium hydroxide; sodium tetrahydroborate; oxalyl dichloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/S0040-4020(88)90018-X

Reference yield:

: 109880-40-2
Methyl 6-formyl-4-methoxypyridine-2-carboxylate

: 108998-85-2
6-<ethyl>-N-(o-nitrophenylthio)amino>methyl>-4-methoxypyridine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent

2: 86 percent / trifluoroacetic acid, Et₃N / CH₂Cl₂ / 0 deg C, 30 min, then RT, 6 h

3: 62 percent / LiOH / tetrahydrofuran / 0 deg C, then RT, 3 h

With lithium hydroxide; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(88)90018-X