(2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric acid

Base Information

Chemical Name:(2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric acid
CAS No.:1621924-52-4
Molecular Formula:C₂₈H₃₀FN₃O₄
Molecular Weight:491.562
Hs Code.:

Synonyms:(2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric acid

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Chemical Property of (2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric acid

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Technology Process of (2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric acid

There total 6 articles about (2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric 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: 89.0%

: 1621924-15-9
(2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-3-carbonyl)amino]butyric acid methyl ester

: 1621924-52-4
(2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric acid

Guidance literature:: With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; for 2h;

Reference yield:

: 132245-78-4
(S)-2-tert-butoxycarbonylaminopentanedioic acid 1-benzyl ester 5-methyl ester

: 1621924-52-4
(2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C

1.2: 1 h / -78 °C

2.1: palladium 10% on activated carbon; hydrogen / methanol / 1 h

3.1: 4-methyl-morpholine; isobutyl chloroformate / toluene / 1 h / 20 °C

4.1: dichloromethane / 5 h

5.1: triethylamine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / dichloromethane; ethyl acetate / 2 h / 0 °C

6.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 2 h

With 4-methyl-morpholine; lithium hydroxide monohydrate; palladium 10% on activated carbon; water; hydrogen; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; lithium hexamethyldisilazane; isobutyl chloroformate; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; toluene;

Reference yield:

: 1621924-48-8
(2S,4S)-2-tert-butoxycarbonylamino-4-methylpentanedioic acid 5-methyl ester

: 1621924-52-4
(2S,4S)-4-[2-(4-fluorophenyl)-1,1-dimethylethylcarbamoyl]-2-methyl-4-[(5-phenylpyridine-2-carbonyl)amino]butyric acid

Guidance literature:: Multi-step reaction with 4 steps

1: 4-methyl-morpholine; isobutyl chloroformate / toluene / 1 h / 20 °C

2: dichloromethane / 5 h

3: triethylamine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / dichloromethane; ethyl acetate / 2 h / 0 °C

4: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 2 h

With 4-methyl-morpholine; lithium hydroxide monohydrate; water; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; isobutyl chloroformate; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; toluene;