2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl ester

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Chemical Name:2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl ester
CAS No.:330641-22-0
Molecular Formula:C₂₂H₃₂N₂O₄S
Molecular Weight:420.573
Hs Code.:

Synonyms:2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl ester

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Chemical Property of 2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl ester

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Technology Process of 2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl ester

There total 5 articles about 2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl 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: 89.0%

: 18598-63-5
L-cysteine methyl ester hydrochloride

: 330641-20-8
(E,E)-8-O-(2-N-methyl-aminobenzoyl)-3,7-dimethyl-2,6-octadiene-1-chloride

: 330641-22-0
2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl ester

Guidance literature:: In tetrahydrofuran; ammonia; at -40 - 20 ℃;
DOI:10.1021/ja002723o

Reference yield:

: 66408-80-8,70238-39-0,80444-67-3,143590-48-1,38290-53-8
(2E,6E)-2,6-dimethyl-8-((tetrahydro-2H-pyran-2-yl)oxy)octa-2,6-dien-1-ol

: 330641-22-0
2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 75 percent / DMAP; Et₃N / dimethylformamide / 3.5 h / 65 °C

2: 92 percent / PPTS / ethanol / 3 h / 60 °C

3: 92 percent / N-chlorosuccinimide; Me₂S / CH₂Cl₂ / 2.25 h / -40 - 20 °C

4: 89 percent / tetrahydrofuran; liquid ammonia / -40 - 20 °C

With dmap; N-chloro-succinimide; dimethylsulfide; pyridinium p-toluenesulfonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; ammonia; N,N-dimethyl-formamide;
DOI:10.1021/ja002723o

Reference yield:

: 10328-92-4
N-Methylisatoic anhydride

: 330641-22-0
2-Methylamino-benzoic acid (2E,6E)-8-((R)-2-amino-2-methoxycarbonyl-ethylsulfanyl)-2,6-dimethyl-octa-2,6-dienyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 75 percent / DMAP; Et₃N / dimethylformamide / 3.5 h / 65 °C

2: 92 percent / PPTS / ethanol / 3 h / 60 °C

3: 92 percent / N-chlorosuccinimide; Me₂S / CH₂Cl₂ / 2.25 h / -40 - 20 °C

4: 89 percent / tetrahydrofuran; liquid ammonia / -40 - 20 °C

With dmap; N-chloro-succinimide; dimethylsulfide; pyridinium p-toluenesulfonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; ammonia; N,N-dimethyl-formamide;
DOI:10.1021/ja002723o