3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid

Base Information

Chemical Name:3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid
CAS No.:848671-17-0
Molecular Formula:C₃₀H₃₇N₃O₄
Molecular Weight:503.641
Hs Code.:

Synonyms:3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid

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Chemical Property of 3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid

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Technology Process of 3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid

There total 6 articles about 3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic 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:

: 56583-58-5,76985-10-9,58438-04-3
N-tert-butoxycarbonyl-3-(2-naphthyl)-L-alanine

: 848671-17-0
3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid

Guidance literature:: Multi-step reaction with 7 steps

1: DCCI; HOBt; NMM / dimethylformamide / 12 h / 20 °C

2: HCl (gas) / CH₂Cl₂ / 2 h / 20 °C

3: DIPEA / methanol / 14 h / 20 °C

4: HATU; DIPEA / dimethylformamide / 48 h / 0 - 20 °C

5: HCl (gas) / CH₂Cl₂ / 2 h / 20 °C

6: Na(OAc)3BH; AcOH / tetrahydrofuran / 1 h / 20 °C

7: LiOH / tetrahydrofuran; H₂O / 1 h / 20 °C

With 4-methyl-morpholine; hydrogenchloride; lithium hydroxide; sodium tris(acetoxy)borohydride; benzotriazol-1-ol; acetic acid; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 3: Michael addition;
DOI:10.1016/j.bmcl.2004.11.072

Reference yield:

: 3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid methyl ester

: 848671-17-0
3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 1h;
DOI:10.1016/j.bmcl.2004.11.072

Reference yield:

: 408540-44-3
3-((S)-1-Methylcarbamoyl-2-naphthalen-2-yl-ethylamino)-propionic acid methyl ester

: 848671-17-0
3-[((S)-2-Benzylamino-4-methyl-pentanoyl)-((S)-1-methylcarbamoyl-2-naphthalen-2-yl-ethyl)-amino]-propionic acid

Guidance literature:: Multi-step reaction with 4 steps

1: HATU; DIPEA / dimethylformamide / 48 h / 0 - 20 °C

2: HCl (gas) / CH₂Cl₂ / 2 h / 20 °C

3: Na(OAc)3BH; AcOH / tetrahydrofuran / 1 h / 20 °C

4: LiOH / tetrahydrofuran; H₂O / 1 h / 20 °C

With hydrogenchloride; lithium hydroxide; sodium tris(acetoxy)borohydride; acetic acid; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2004.11.072