tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate
CAS No.:521975-55-3
Molecular Formula:C₃₆H₄₅N₃O₅
Molecular Weight:599.77
Hs Code.:

Synonyms:tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate

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Chemical Property of tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate

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Technology Process of tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate

There total 6 articles about tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate 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: 85.0%

: 1-[3-(2-methoxyphenoxy)benzyl]piperidin-4-ylamine dihydrochloride

: 167262-68-2
N-(t-butyloxycarbonyl)-4-phenylpiperidine-4-carboxylic acid

: 521975-55-3
tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1021/jm050965z

Reference yield:

: 1-{[3-(2-methoxyphenoxy)benzyl]piperidin-4-yl}carbamic acid tert-butyl ester

: 521975-55-3
tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / aq. HCl / dioxane / 2 h / 20 °C

2: 85 percent / HOBt; EDCI / CH₂Cl₂ / 5 h / 20 °C

With hydrogenchloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; dichloromethane;
DOI:10.1021/jm050965z

Reference yield:

: 66855-92-3
3-(2-methoxyphenoxy)benzaldehyde

: 521975-55-3
tert-butyl-4-((1-(3-(2-methoxyphenoxy)benzyl)piperidin-4-yl)carbamoyl)-4-phenylpiperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: Na(OAc)3BH; AcOH / 1,2-dichloro-ethane / 20 °C

2: 91 percent / aq. HCl / dioxane / 2 h / 20 °C

3: 85 percent / HOBt; EDCI / CH₂Cl₂ / 5 h / 20 °C

With hydrogenchloride; sodium tris(acetoxy)borohydride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/jm050965z