2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester

Base Information

Chemical Name:2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester
CAS No.:910301-25-6
Molecular Formula:C₃₅H₄₈N₄O₇
Molecular Weight:636.789
Hs Code.:

2-{5-<i>tert</i>-butoxycarbonylamino-1-[2-(1<i>H</i>-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester

Synonyms:2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester

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Chemical Property of 2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester

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Technology Process of 2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester

There total 4 articles about 2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl 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: 74.0%

: 204501-99-5
6-tert-butoxycarbonylamino-2-(1-ethoxycarbonyl-3-phenyl-propylamino)-hexanoic acid

: 4299-70-1
L-tryptophan methyl ester

: 910301-25-6
2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 72h;
DOI:10.1016/j.bmcl.2006.06.004

Reference yield:

: 2418-95-3
(S)-2-amino-6-(tert-butoxycarbonylamino)hexanoic acid

: 910301-25-6
2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₃CN / ethanol; H₂O / 12 h / 20 °C

2: 74 percent / EDC*HCl; HOBt; diisopropylethylamine / dimethylformamide / 72 h / 20 °C

With sodium cyanoborohydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2006.06.004

Reference yield:

: 64920-29-2
2-oxo-4-phenylbutanoic acid ethyl ester

: 910301-25-6
2-{5-tert-butoxycarbonylamino-1-[2-(1H-indol-3-yl)-1-methoxycarbonyl-ethylcarbamoyl]-pentylamino}-4-phenyl-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₃CN / ethanol; H₂O / 12 h / 20 °C

2: 74 percent / EDC*HCl; HOBt; diisopropylethylamine / dimethylformamide / 72 h / 20 °C

With sodium cyanoborohydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2006.06.004