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(S)-5-(benzyloxycarbonylamino)-2-(tert-butoxycarbonylamino)pentylmethanesulfonate

Base Information
  • Chemical Name:(S)-5-(benzyloxycarbonylamino)-2-(tert-butoxycarbonylamino)pentylmethanesulfonate
  • CAS No.:233689-91-3
  • Molecular Formula:C19H30N2O7S
  • Molecular Weight:430.522
  • Hs Code.:
(S)-5-(benzyloxycarbonylamino)-2-(tert-butoxycarbonylamino)pentylmethanesulfonate

Synonyms:(S)-5-(benzyloxycarbonylamino)-2-(tert-butoxycarbonylamino)pentylmethanesulfonate

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Chemical Property of (S)-5-(benzyloxycarbonylamino)-2-(tert-butoxycarbonylamino)pentylmethanesulfonate
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Technology Process of (S)-5-(benzyloxycarbonylamino)-2-(tert-butoxycarbonylamino)pentylmethanesulfonate

There total 3 articles about (S)-5-(benzyloxycarbonylamino)-2-(tert-butoxycarbonylamino)pentylmethanesulfonate 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:
Guidance literature:
Boc-Orn(Z)-OH; With 4-methyl-morpholine; isobutyl chloroformate; In tetrahydrofuran; at -15 ℃; for 0.166667h;
With sodium tetrahydroborate; In tetrahydrofuran; water; for 0.166667h; Cooling with ice;
methanesulfonyl chloride; With triethylamine; In dichloromethane; at 20 ℃; for 0.5h; Cooling with ice;
Guidance literature:
Multi-step reaction with 2 steps
1.1: ethyl chloroformate / tetrahydrofuran / 0.25 h / -10 - 0 °C
1.2: 83 percent / NaBH4 / tetrahydrofuran; methanol / 0 °C
2.1: 80 percent / triethylamine / CH2Cl2 / 1.5 h / 0 - 20 °C
With chloroformic acid ethyl ester; triethylamine; In tetrahydrofuran; dichloromethane; 1.1: Substitution / 1.2: Reduction / 2.1: Substitution;
DOI:10.1002/1099-0690(200004)2000:7<1219::AID-EJOC1219>3.0.CO;2-P
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