(R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride

Base Information

Chemical Name:(R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride
CAS No.:1322746-39-3
Molecular Formula:C₁₈H₂₅N₃O₆*ClH
Molecular Weight:415.874
Hs Code.:

Synonyms:(R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride

Suppliers and Price of (R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride

There total 4 articles about (R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride 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: 41.3%

: (R)-2-tert-butoxycarbonylamino-5-(piperidin-4-yl)pentanoic acid acetate

: 4457-32-3
4-nitrobenzyl chloroformate

: 1322746-39-3
(R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride

Guidance literature:: (R)-2-tert-butoxycarbonylamino-5-(piperidin-4-yl)pentanoic acid acetate; 4-nitrobenzyl chloroformate; With sodium hydroxide; In 1,4-dioxane; water; at 0 - 20 ℃; pH=8 - 9;

With hydrogenchloride; In water; acetic acid; at 20 ℃; for 1h;

Reference yield:

: 170899-08-8
N-(tert-butoxycarbonyl)-D-allylglycine

: 1322746-39-3
(R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate / palladium diacetate / N,N-dimethyl-formamide; water / 20 °C

2.1: hydrogen / Adam’s catalyst / ethanol; water / 20 °C / Inert atmosphere

3.1: sodium hydroxide / 1,4-dioxane; water / 0 - 20 °C / pH 8 - 9

3.2: 1 h / 20 °C

With hydrogen; sodium hydrogencarbonate; sodium hydroxide; Adam’s catalyst; palladium diacetate; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1322746-34-8
(R,E)-2-tert-butyloxycarbonylamino-5-(pyridine-4-yl)pent-4-enoic acid

: 1322746-39-3
(R)-2-amino-5-(1-(4-nitrobenzyloxy)carbonylpiperidin-4-yl)pentanoic acid hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen / Adam’s catalyst / ethanol; water / 20 °C / Inert atmosphere

2.1: sodium hydroxide / 1,4-dioxane; water / 0 - 20 °C / pH 8 - 9

2.2: 1 h / 20 °C

With hydrogen; sodium hydroxide; Adam’s catalyst; In 1,4-dioxane; ethanol; water;