{(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

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Chemical Name:{(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester
CAS No.:180463-07-4
Molecular Formula:C₃₂H₄₈N₄O₆
Molecular Weight:584.756
Hs Code.:

Synonyms:{(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

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Chemical Property of {(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

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Technology Process of {(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

There total 7 articles about {(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic 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: 80.0%

: 98760-08-8
(2R,3S)-3-[N-(tert-butyloxycarbonyl)amino]-1,2-epoxy-4-phenylbutane

: 180463-06-3
[(S)-1-(N'-Isobutyl-hydrazinocarbonyl)-2-methyl-propyl]-carbamic acid benzyl ester

: 180463-07-4
{(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

Guidance literature:: In ethanol; at 80 ℃; for 16h;
DOI:10.1021/jm960022p

Reference yield:

: 72-18-4,25609-85-2,7004-03-7,921-10-8
L-valine

: 180463-07-4
{(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 2 N aq. NaOH / dioxane / 16 h / Ambient temperature

2: 1.) 4-methylmorpholine, 1-ethyl-3-(3-diaminopropyl)carbodiimide hydrochloride, 1-hydroxybenzotriazole hydrate / 1.) AcOEt, 10 min, 2.) AcOEt, 18 h

3: 92 percent / HCl(gas) / dioxane / 28 h

4: 87 percent / ethanol / 4 h / 60 °C

5: 87 percent / p-TsOH, NaBH₃CN / tetrahydrofuran / 1 h / Ambient temperature

6: 80 percent / ethanol / 16 h / 80 °C

With 4-methyl-morpholine; hydrogenchloride; sodium hydroxide; 1-ethyl-3-(3-diaminopropyl)carbodiimide hydrochloride; sodium cyanoborohydride; toluene-4-sulfonic acid; 1-hydroxybenzotriazol-hydrate; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1021/jm960022p

Reference yield:

: 1149-26-4
(S)-N-(benzyloxycarbonyl)valine

: 180463-07-4
{(1S,2S)-1-Benzyl-3-[N'-((S)-2-benzyloxycarbonylamino-3-methyl-butyryl)-N-isobutyl-hydrazino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) 4-methylmorpholine, 1-ethyl-3-(3-diaminopropyl)carbodiimide hydrochloride, 1-hydroxybenzotriazole hydrate / 1.) AcOEt, 10 min, 2.) AcOEt, 18 h

2: 92 percent / HCl(gas) / dioxane / 28 h

3: 87 percent / ethanol / 4 h / 60 °C

4: 87 percent / p-TsOH, NaBH₃CN / tetrahydrofuran / 1 h / Ambient temperature

5: 80 percent / ethanol / 16 h / 80 °C

With 4-methyl-morpholine; hydrogenchloride; 1-ethyl-3-(3-diaminopropyl)carbodiimide hydrochloride; sodium cyanoborohydride; toluene-4-sulfonic acid; 1-hydroxybenzotriazol-hydrate; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1021/jm960022p