tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate

Base Information

Chemical Name:tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate
CAS No.:1313216-85-1
Molecular Formula:C₃₄H₄₅N₃O₆S
Molecular Weight:623.814
Hs Code.:

Synonyms:tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate

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Chemical Property of tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate

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Technology Process of tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate

There total 5 articles about tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate 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: 81.0%

: 1187450-49-2
tert-butyl (tert-butoxycarbonyl(6-(hydroxymethyl)pyridin-2-yl)amino)acetate

: 1022379-81-2
N-(4-tert-butylbenzyl)benzenesulfonamide

: 1313216-85-1
tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate

Guidance literature:: With tributylphosphine; diamide; In tetrahydrofuran; at 20 ℃; for 2.5h;

Reference yield:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 1313216-85-1
tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1.33 h / 20 °C / Inert atmosphere; Cooling with ice

1.2: 1.17 h / 20 °C / Cooling with ice

2.1: calcium chloride; potassium borohydride / Tetraethylene glycol dimethyl ether; ethanol / 0.92 h / 20 - 35 °C / Cooling with ice

2.2: 1.17 h / 20 °C / Cooling with ice

3.1: tributylphosphine; diamide / tetrahydrofuran / 2.5 h / 20 °C

With potassium borohydride; tributylphosphine; diamide; sodium hydride; calcium chloride; In tetrahydrofuran; ethanol; Tetraethylene glycol dimethyl ether; N,N-dimethyl-formamide; mineral oil; 3.1: Mitsunobu reaction;

Reference yield:

: 1187451-25-7
tert-butyl [tert-butoxycarbonyl(6-ethoxycarbonylpyridine-2-yl)amino]acetate

: 1313216-85-1
tert-butyl ((6-((phenylsulfonyl)(4-tert-butylbenzyl)aminomethyl)pyridin-2-yl)(tert-butoxycarbonyl)amino)acetate

Guidance literature:: Multi-step reaction with 2 steps

1.1: calcium chloride; potassium borohydride / Tetraethylene glycol dimethyl ether; ethanol / 0.92 h / 20 - 35 °C / Cooling with ice

1.2: 1.17 h / 20 °C / Cooling with ice

2.1: tributylphosphine; diamide / tetrahydrofuran / 2.5 h / 20 °C

With potassium borohydride; tributylphosphine; diamide; calcium chloride; In tetrahydrofuran; ethanol; Tetraethylene glycol dimethyl ether; 2.1: Mitsunobu reaction;