N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine

Base Information

Chemical Name:N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine
CAS No.:1432294-01-3
Molecular Formula:C₂₈H₃₃ClN₈O₂
Molecular Weight:549.075
Hs Code.:

Synonyms:N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine

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Chemical Property of N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine

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Technology Process of N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine

There total 7 articles about N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine 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:

: 1432293-21-4
N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N’-(4-phenethyl-piperidin-4-yl)methylguanidine

: 103-80-0
phenylacetyl chloride

: 1432294-01-3
N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 4878-36-8
3,5-diamino-6-chloro-pyrazine-2-carboxylic acid

: 1432294-01-3
N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine

Guidance literature:: Multi-step reaction with 5 steps

1.1: trifluorormethanesulfonic acid / 1 h / Cooling with ice

1.2: 4 h / 20 °C / Cooling with ice

2.1: sodium hydroxide; water / tert-butyl methyl ether; tetrahydrofuran / 20 °C

3.1: acetonitrile / 48 h / 70 °C

4.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

With trifluorormethanesulfonic acid; water; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; dichloromethane; tert-butyl methyl ether; acetonitrile;

Reference yield:

: 1458-01-1
3,5-diamino-6-chloro-pyrazine-2-carboxylic acid methyl ester

: 1432294-01-3
N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-(4-phenethyl-1-phenylacetyl-piperidin-4-ylmethyl)-guanidine

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide; water / methanol / 3 h / Reflux

2.1: trifluorormethanesulfonic acid / 1 h / Cooling with ice

2.2: 4 h / 20 °C / Cooling with ice

3.1: sodium hydroxide; water / tert-butyl methyl ether; tetrahydrofuran / 20 °C

4.1: acetonitrile / 48 h / 70 °C

5.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

With trifluorormethanesulfonic acid; water; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; tert-butyl methyl ether; acetonitrile;