(S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic acid methyl ester

Base Information

• Chemical Name: (S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic acid methyl ester
• CAS No.: 128632-75-7
• Molecular Formula: C₄₅H₅₅N₇O₉
• Molecular Weight: 837.973

Synonyms:(S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic acid methyl ester

Chemical Property of (S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic acid methyl ester

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Technology Process of (S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic acid methyl ester

There total 5 articles about (S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic 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:

Z-Asp-D-Phe-Lys-D-Trp-Leu-OMe*HCl (128633-14-7) → (S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic acid methyl ester (128632-75-7)

Guidance literature:

With diphenyl phosphoryl azide; sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 4 ℃; for 72h; Yield given;

DOI:10.1021/jm00171a033

Reference yield:

N-benzyloxycarbonyl-D-phenylalanyl-L-lysyl(Boc)-D-tryptophyl-L-leucine methyl ester (128633-07-8) → (S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic acid methyl ester (128632-75-7)

Guidance literature:

Multi-step reaction with 4 steps

1: H₂ / 5percent Pd-C / ethanol / 5 h

2: 84 percent / dimethylformamide / 48 h / Ambient temperature

3: HCl, acetic acid

4: diphenyl phosphorazidate, NaHCO₃ / dimethylformamide / 72 h / 4 °C

With hydrogenchloride; diphenyl phosphoryl azide; hydrogen; sodium hydrogencarbonate; acetic acid; palladium on activated charcoal; In ethanol; N,N-dimethyl-formamide;

DOI:10.1021/jm00171a033

Reference yield:

Z-Asp(OtBu)-OSu (3338-32-7) → (S)-2-[(R)-2-[((3R,6S,14S)-3-Benzyl-6-benzyloxycarbonylamino-2,5,8-trioxo-1,4,9-triaza-cyclotetradecane-14-carbonyl)-amino]-3-(1H-indol-3-yl)-propionylamino]-4-methyl-pentanoic acid methyl ester (128632-75-7)

Guidance literature:

Multi-step reaction with 3 steps

1: 84 percent / dimethylformamide / 48 h / Ambient temperature

2: HCl, acetic acid

3: diphenyl phosphorazidate, NaHCO₃ / dimethylformamide / 72 h / 4 °C

With hydrogenchloride; diphenyl phosphoryl azide; sodium hydrogencarbonate; acetic acid; In N,N-dimethyl-formamide;

DOI:10.1021/jm00171a033

upstream raw materials:

Z-Asp-D-Phe-Lys-D-Trp-Leu-OMe*HCl

Z-Asp(OtBu)-OSu

Z-Asp(OBu^t)-D-Phe-Lys(Boc)-D-Trp-Leu-OMe

N-benzyloxycarbonyl-D-phenylalanyl-L-lysyl(Boc)-D-tryptophyl-L-leucine methyl ester

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