2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid

Base Information

Chemical Name:2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid
CAS No.:1259040-06-6
Molecular Formula:C₃₀H₄₃N₇O₂
Molecular Weight:533.717
Hs Code.:

Synonyms:2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid

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Chemical Property of 2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid

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Technology Process of 2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid

There total 6 articles about 2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid 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:

: 1259040-11-3
C₃₂H₄₇N₇O₂

: 1259040-06-6
2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid

Guidance literature:: C₃₂H₄₇N₇O₂; With water; sodium hydroxide; In ethanol; at 70 ℃; for 25h;

With hydrogenchloride; In water;

Reference yield:

tert-butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate: 135716-08-4
tert-butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate

: 1259040-06-6
2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: trifluoroacetic acid / toluene / 40 h / Inert atmosphere

2.1: hydrogenchloride / ethyl acetate; ethanol / 1.33 h / 20 °C

3.1: titanium(IV) tetraethanolate / 1 h / 50 °C / Inert atmosphere

3.2: 0.67 h / Inert atmosphere

3.3: 0.5 h / 20 °C

4.1: hydrogen; acetic acid / palladiumcarbon hydroxide / N,N-dimethyl-formamide; ethanol / 1 h / 50 °C

5.1: acetic acid; sodium tris(acetoxy)borohydride / N,N-dimethyl-formamide / 1 h / Inert atmosphere

6.1: sodium hydroxide; water / ethanol / 25 h / 70 °C

With hydrogenchloride; titanium(IV) tetraethanolate; water; hydrogen; sodium tris(acetoxy)borohydride; acetic acid; trifluoroacetic acid; sodium hydroxide; palladiumcarbon hydroxide; In ethanol; ethyl acetate; N,N-dimethyl-formamide; toluene;

Reference yield:

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 1259040-06-6
2-(4-{[bis(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-8-(1-ethylpropyl)-2,8-diazaspiro[4.5]decane-4-carboxylic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydride / tetrahydrofuran / 0.33 h / 0 °C / Inert atmosphere

1.2: 3 h / 20 °C

2.1: trifluoroacetic acid / toluene / 40 h / Inert atmosphere

3.1: hydrogenchloride / ethyl acetate; ethanol / 1.33 h / 20 °C

4.1: titanium(IV) tetraethanolate / 1 h / 50 °C / Inert atmosphere

4.2: 0.67 h / Inert atmosphere

4.3: 0.5 h / 20 °C

5.1: hydrogen; acetic acid / palladiumcarbon hydroxide / N,N-dimethyl-formamide; ethanol / 1 h / 50 °C

6.1: acetic acid; sodium tris(acetoxy)borohydride / N,N-dimethyl-formamide / 1 h / Inert atmosphere

7.1: sodium hydroxide; water / ethanol / 25 h / 70 °C

With hydrogenchloride; titanium(IV) tetraethanolate; water; hydrogen; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; trifluoroacetic acid; sodium hydroxide; palladiumcarbon hydroxide; In tetrahydrofuran; ethanol; ethyl acetate; N,N-dimethyl-formamide; toluene;