(S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester

Base Information

Chemical Name:(S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester
CAS No.:189279-99-0
Molecular Formula:C₂₅H₄₁ClN₂O₅
Molecular Weight:485.064
Hs Code.:

Synonyms:(S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester

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Chemical Property of (S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester

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Technology Process of (S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester

There total 5 articles about (S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl 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: 77.0%

: 67843-74-7,24969-06-0,13403-37-7
(S)-epichlorohydrin

: 189279-95-6
(S)-t-Boc-Lys(Bz)-O-t-Bu

: 189279-99-0
(S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester

Guidance literature:: With magnesium sulfate; In methanol; for 72h;
DOI:10.1021/jo970119z

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 189279-99-0
(S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaHCO₃ / 1.) H₂O, CHCl₃, room temperature, 5 min, 2.) CHCl₃, reflux, 1.5 h.

2: 99 percent / H₂, 1N HCl / ethanol / 12 h

4: 77 percent / MgSO₄ / methanol / 72 h

With hydrogenchloride; hydrogen; sodium hydrogencarbonate; magnesium sulfate; In methanol; ethanol;
DOI:10.1021/jo970119z

Reference yield:

: 5978-22-3,1426213-63-9
N(ε)-benzoyloxycarbonyl-L-lysine tert-butyl ester hydrochloride

: 189279-99-0
(S)-6-[Benzyl-((S)-3-chloro-2-hydroxy-propyl)-amino]-2-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaHCO₃ / 1.) H₂O, CHCl₃, room temperature, 5 min, 2.) CHCl₃, reflux, 1.5 h.

2: 99 percent / H₂, 1N HCl / ethanol / 12 h

4: 77 percent / MgSO₄ / methanol / 72 h

With hydrogenchloride; hydrogen; sodium hydrogencarbonate; magnesium sulfate; In methanol; ethanol;
DOI:10.1021/jo970119z