N₁-(1,2,3,4-tetrahydroacridin-9-yl)-N₆-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine

Base Information

• Chemical Name: N₁-(1,2,3,4-tetrahydroacridin-9-yl)-N₆-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine
• CAS No.: 1268720-50-8
• Molecular Formula: C₂₉H₃₉N₃O₃
• Molecular Weight: 477.647

Synonyms:N₁-(1,2,3,4-tetrahydroacridin-9-yl)-N₆-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine

Chemical Property of N₁-(1,2,3,4-tetrahydroacridin-9-yl)-N₆-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine

Chemical Property:

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Technology Process of N₁-(1,2,3,4-tetrahydroacridin-9-yl)-N₆-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine

There total 5 articles about N₁-(1,2,3,4-tetrahydroacridin-9-yl)-N₆-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine 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:

C29H37N3O3 → N1-(1,2,3,4-tetrahydroacridin-9-yl)-N6-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine (1268720-50-8)

Guidance literature:

With sodium tetrahydroborate; In methanol; at 20 ℃; for 4h;

DOI:10.1016/j.bmc.2010.12.022

Reference yield:

spiro<2H-3,1-benzoxazine-2,1'-cyclohexan>-4(1H)-one (96447-10-8) → N1-(1,2,3,4-tetrahydroacridin-9-yl)-N6-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine (1268720-50-8)

Guidance literature:

Multi-step reaction with 4 steps

1: trichlorophosphate / 120 °C

2: potassium iodide / pentan-1-ol / 10 h / 160 °C / Reflux

3: methanol / 4 h / 20 °C

4: sodium tetrahydroborate / methanol / 4 h / 20 °C

With sodium tetrahydroborate; potassium iodide; trichlorophosphate; In methanol; pentan-1-ol;

DOI:10.1016/j.bmc.2010.12.022

Reference yield:

9-chloro-1,2,3,4-tetrahydroacridine (5396-30-5) → N1-(1,2,3,4-tetrahydroacridin-9-yl)-N6-(3,4,5-trimethoxybenzyl)hexane-1,6-diamine (1268720-50-8)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium iodide / pentan-1-ol / 10 h / 160 °C / Reflux

2: methanol / 4 h / 20 °C

3: sodium tetrahydroborate / methanol / 4 h / 20 °C

With sodium tetrahydroborate; potassium iodide; In methanol; pentan-1-ol;

DOI:10.1016/j.bmc.2010.12.022

upstream raw materials:

spiro<2H-3,1-benzoxazine-2,1'-cyclohexan>-4(1H)-one

9-chloro-1,2,3,4-tetrahydroacridine

cyclohexanone

anthranilic acid

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