7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide

Base Information

Chemical Name:7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide
CAS No.:714249-18-0
Molecular Formula:C₂₃H₂₇N₅O₂S
Molecular Weight:437.566
Hs Code.:

Synonyms:7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide

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Chemical Property of 7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide

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Technology Process of 7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide

There total 4 articles about 7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide 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: 32.0%

: 714249-06-6
tert-butyl 4-{4-[[(7-cyano-2-napthyl)methyl](methylsulfonyl)amino]phenyl}piperazine-1-carboxylate

: 714249-18-0
7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide

Guidance literature:: tert-butyl 4-{4-[[(7-cyano-2-napthyl)methyl](methylsulfonyl)amino]phenyl}piperazine-1-carboxylate; With hydrogenchloride; ethanol; at 5 ℃; for 15h;

With ammonium acetate; In ethanol; at 20 ℃; for 24h;
DOI:10.1016/j.bmc.2004.02.022

Reference yield:

: 182618-86-6
tert-butyl 4-(4-nitrophenyl)piperazine-1-carboxylate

: 714249-18-0
7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: H₂ / Pd/C / ethanol / 16 h / 20 °C

2.1: acetic acid; sodium triacetoxyborohydride / 1,2-dichloro-ethane / 5 h

3.1: 65 percent / pyridine / 1,2-dichloro-ethane / 12 h / 20 °C

4.1: hydrogen chloride; ethanol / 15 h / 5 °C

4.2: 32 percent / ammonium acetate / ethanol / 24 h / 20 °C

With pyridine; hydrogenchloride; ethanol; hydrogen; sodium tris(acetoxy)borohydride; acetic acid; palladium on activated charcoal; In ethanol; 1,2-dichloro-ethane;
DOI:10.1016/j.bmc.2004.02.022

Reference yield:

: 170911-92-9
4-(4-aminophenyl)-1-t-butyloxycarbonylpiperazine

: 714249-18-0
7-({(methylsulfonyl)[4-(piperazin-1-yl)phenyl]amino}methyl)naphthalene-2-carboximidamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetic acid; sodium triacetoxyborohydride / 1,2-dichloro-ethane / 5 h

2.1: 65 percent / pyridine / 1,2-dichloro-ethane / 12 h / 20 °C

3.1: hydrogen chloride; ethanol / 15 h / 5 °C

3.2: 32 percent / ammonium acetate / ethanol / 24 h / 20 °C

With pyridine; hydrogenchloride; ethanol; sodium tris(acetoxy)borohydride; acetic acid; In 1,2-dichloro-ethane;
DOI:10.1016/j.bmc.2004.02.022