[3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

Base Information

Chemical Name:[3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester
CAS No.:193073-99-3
Molecular Formula:C₂₀H₂₂FN₃O₆
Molecular Weight:419.41
Hs Code.:

Synonyms:[3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

Suppliers and Price of [3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of [3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of [3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

There total 14 articles about [3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl 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: 94.0%

: 193073-96-0
[(2S)-2-(tert-butoxycarbonylmethylamino)-3-(4-fluoro-3-nitrophenyl)propionylamino]-(R)-(4-methoxyphenyl)methyl ester

: 193073-99-3
[3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

Guidance literature:: With chloro-trimethyl-silane; sodium iodide; In chloroform; at 20 ℃; for 0.166667h;
DOI:10.3987/COM-99-8514

Reference yield:

: 42564-51-2
4-fluoro-3-nitrobenzaldehyde

: 193073-99-3
[3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 98 percent / NaBH₄ / methanol

2: 82 percent / PBr₃ / toluene

3: 54 percent / n-C₄H₉Li; CuCN / tetrahydrofuran / 20 °C

4: 65 percent / TFA / acetonitrile; H₂O

5: 54 percent / N(C₂H₅)3 / tetrahydrofuran / 16 h / 20 °C

6: 83 percent / Ag₂O / dimethylformamide / 60 h / 60 °C

7: 90 percent / K₂CO₃; H₂O / methanol / 6 h / 20 °C

8: 92 percent / N(C₂H₅)3; EDC; HOBT / CH₂Cl₂ / 2 h / 20 °C

9: 94 percent / NaI; TMSCl / CHCl₃ / 0.17 h / 20 °C

With sodium tetrahydroborate; n-butyllithium; chloro-trimethyl-silane; water; phosphorus tribromide; potassium carbonate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; trifluoroacetic acid; sodium iodide; silver(l) oxide; In tetrahydrofuran; methanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide; toluene; acetonitrile; 1: Reduction / 2: Bromination / 3: Alkylation / 4: Hydrolysis / 5: Acylation / 6: Methylation / 7: Hydrolysis / 8: Acylation / 9: deacylation;
DOI:10.3987/COM-99-8514

Reference yield:

: (R)-(3,5-dichloro-4-methoxy)phenylglycine methyl ester hydrochloride

: 193073-99-3
[3-(4-fluoro-3-nitrophenyl)-(2S)-2-methylaminopropionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / H₂ / Pd/C / methanol

2: 92 percent / N(C₂H₅)3; EDC; HOBT / CH₂Cl₂ / 2 h / 20 °C

3: 94 percent / NaI; TMSCl / CHCl₃ / 0.17 h / 20 °C

With chloro-trimethyl-silane; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; sodium iodide; palladium on activated charcoal; In methanol; dichloromethane; chloroform; 1: Dehalogenation / 2: Acylation / 3: deacylation;
DOI:10.3987/COM-99-8514