N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide

Base Information

• Chemical Name: N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide
• CAS No.: 155290-48-5
• Molecular Formula: C₂₇H₃₆N₆O₃S
• Molecular Weight: 524.687
• Mol file: 155290-48-5.mol

Synonyms:N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide

Chemical Property of N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide

There total 4 articles about N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide 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:

1-(4-aminobutyl)-4-(1,2-benzisothiazol-3-yl)piperazine (105981-34-8) + C17H24N2O6 → N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide (155290-48-5)

Guidance literature:

With triethylamine; In tetrahydrofuran; at -30 - -15 ℃; for 0.75h; Yield given;

DOI:10.1021/jm950551d

Reference yield:

di-tert-butyl dicarbonate (24424-99-5) → N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide (155290-48-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 91 percent / 5percent aq. Na₂CO₃ / dioxane / 32 h / Ambient temperature

2: Et₃N / tetrahydrofuran / 0.08 h / -35 - -20 °C

3: Et₃N / tetrahydrofuran / 0.75 h / -30 - -15 °C

With sodium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane;

DOI:10.1021/jm950551d

Reference yield:

2-hydrazinobenzoic acid hydrochloride (33906-30-8,52356-01-1) → N-{4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl}-2-[2-(tert-butoxycarbonyl)hydrazino]benzamide (155290-48-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 91 percent / 5percent aq. Na₂CO₃ / dioxane / 32 h / Ambient temperature

2: Et₃N / tetrahydrofuran / 0.08 h / -35 - -20 °C

3: Et₃N / tetrahydrofuran / 0.75 h / -30 - -15 °C

With sodium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane;

DOI:10.1021/jm950551d

upstream raw materials:

1-(4-aminobutyl)-4-(1,2-benzisothiazol-3-yl)piperazine

di-tert-butyl dicarbonate

2-hydrazinobenzoic acid hydrochloride

2-[2-(tert-butoxycarbonyl)hydrazinyl]benzoic acid