(4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

Base Information

Chemical Name:(4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester
CAS No.:847934-50-3
Molecular Formula:C₃₆H₄₉N₄O₈P
Molecular Weight:696.781
Hs Code.:

(4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

Synonyms:(4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

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Chemical Property of (4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

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Technology Process of (4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

There total 1 articles about (4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl 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: 61.0%

: 284677-41-4
(S)-asparagine-3-((1-naphthyl)propyl)amide

: 690254-42-3
(2S)-2-(tert-butyloxycarbonyl)amino-3-(4-diethylphosphono)phenylpropionic acid

: 847934-50-3
(4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 24h;
DOI:10.1021/jm0492709

Reference yield:

: 847934-50-3
(4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

: (4-{(S)-2-Amino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

Guidance literature:: With methoxybenzene; trifluoroacetic acid; at 20 ℃; for 2h;
DOI:10.1021/jm0492709

Reference yield:

: 847934-50-3
(4-{(S)-2-tert-Butoxycarbonylamino-2-[(S)-2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-propyl}-phenyl)-phosphonic acid diethyl ester

: (R)-N-[(S)-1-[(S)-2-Carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-1-methyl-2-(4-phosphono-phenyl)-ethyl]-3-(4-phosphonomethyl-benzyl)-succinamic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluoroacetic acid; anisole / 2 h / 20 °C

2.1: 260 mg / tetramethylfluoroformamidinium hexafluorophosphate; i-Pr₂NEt / dimethylformamide / 48 h / 20 °C

3.1: thioanisole; trimethylsilyliodide / acetonitrile / 1.5 h / 0 - 20 °C

3.2: 55 percent / aq. trifluoroacetic acid / 2 h / 20 °C

With trimethylsilyl iodide; methyl-phenyl-thioether; methoxybenzene; N-ethyl-N,N-diisopropylamine; fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate; trifluoroacetic acid; In N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm0492709