(5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate

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Chemical Name:(5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate
CAS No.:1374040-17-1
Molecular Formula:C₄₅H₆₄ClN₅O₁₂
Molecular Weight:902.482
Hs Code.:

(5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate

Synonyms:(5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate

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Chemical Property of (5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate

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Technology Process of (5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate

There total 2 articles about (5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate 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: 33.0%

: 1374040-16-0
(5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(hydroxymethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate

: 1374040-17-1
(5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate

Guidance literature:: With thionyl chloride; triethylamine; In benzene; at 20 ℃; for 6h; Cooling with ice;

Reference yield:

: 1374040-14-8
(R)-tert-butyl 3-amino-4-(4-(hydroxymethyl)phenylamino)-4-oxobutanoate

: 1374040-17-1
(5S,8S,11R,14R)-tert-butyl 5-(2-tert-butoxy-2-oxoethyl)-8-(3-tert-butoxy-3-oxopropyl)-14-(4-(chloromethyl)phenylcarbamoyl)-11-isopropyl-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate

Guidance literature:: Multi-step reaction with 2 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 18 h

2: thionyl chloride; triethylamine / benzene / 6 h / 20 °C / Cooling with ice

With thionyl chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; benzene;