9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid methyl ester

Base Information

Chemical Name:9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid methyl ester
CAS No.:215611-40-8
Molecular Formula:C₃₂H₄₆N₂O₇
Molecular Weight:570.726
Hs Code.:

Synonyms:9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid methyl ester

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Chemical Property of 9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid methyl ester

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Technology Process of 9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid methyl ester

There total 2 articles about 9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic 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:

: 818-88-2
sebacic acid mono methyl ester

: 215611-40-8
9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / tetrahydrofuran / 0.5 h / 0 °C

2: tetrahydrofuran / 0.5 h

With triethylamine; In tetrahydrofuran;
DOI:10.1002/(SICI)1521-3765(19980904)4:9<1698::AID-CHEM1698>3.0.CO;2-J

Reference yield:

: 10-Isobutoxycarbonyloxy-10-oxo-decanoic acid methyl ester

: [(S)-2-(4-Benzyloxy-phenyl)-1-hydroxyaminomethyl-ethyl]-carbamic acid tert-butyl ester

: 215611-40-8
9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid methyl ester

Guidance literature:: In tetrahydrofuran; for 0.5h; Yield given;
DOI:10.1002/(SICI)1521-3765(19980904)4:9<1698::AID-CHEM1698>3.0.CO;2-J

Reference yield: 99.0%

: 215611-40-8
9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid methyl ester

: 9-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-nonanoic acid

Guidance literature:: With lithium hydroxide; water; In tetrahydrofuran; methanol; for 0.5h;
DOI:10.1002/(SICI)1521-3765(19980904)4:9<1698::AID-CHEM1698>3.0.CO;2-J