(S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester

Base Information

Chemical Name:(S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester
CAS No.:1610619-91-4
Molecular Formula:C₂₀H₂₅ClN₈O₃
Molecular Weight:460.923
Hs Code.:

Synonyms:(S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester

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Chemical Property of (S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester

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Technology Process of (S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester

There total 5 articles about (S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester 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:

: 1583272-58-5
N-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-N'-piperidin-3-yl-guanidine

: 1129-28-8
3-methoxycarbonylbenzyl bromide

: 1610619-91-4
(S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 6h;

Reference yield:

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

: 1610619-91-4
(S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: trifluorormethanesulfonic acid / tert-butyl alcohol / 1 h / Cooling with ice

1.2: 4 h / 20 °C

2.1: sodium hydroxide / water; dichloromethane; tetrahydrofuran / 20 °C

3.1: triethylamine / N,N-dimethyl-formamide; isopropyl alcohol / 70 °C

3.2: 2 h / 20 °C

4.1: triethylamine / N,N-dimethyl-formamide / 6 h / 20 °C

With trifluorormethanesulfonic acid; triethylamine; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; isopropyl alcohol; tert-butyl alcohol;

Reference yield:

: 775530-61-5
3,5-diamino-6-chloro-N-[(methylsulfanyl)methanimidoyl]pyrazine-2-carboxamide

: 1610619-91-4
(S)-3-{3-[N'-(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / N,N-dimethyl-formamide; isopropyl alcohol / 70 °C

1.2: 2 h / 20 °C

2.1: triethylamine / N,N-dimethyl-formamide / 6 h / 20 °C

With triethylamine; In N,N-dimethyl-formamide; isopropyl alcohol;