N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ⁵-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide

Base Information

• Chemical Name: N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ⁵-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide
• CAS No.: 699023-41-1
• Molecular Formula: C₁₇H₂₆N₃O₃PS
• Molecular Weight: 383.452

Synonyms:N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ⁵-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide

Chemical Property of N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ⁵-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide

Chemical Property:

Purity/Quality:

98% ^*data from raw suppliers

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Technology Process of N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ⁵-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide

There total 3 articles about N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ⁵-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide 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: 89.0%

4-toluenesulfonyl azide (941-55-9) + (1,3-dimethyl-[1,3,2]diazaphospholidin-2-yl)-dimethyl-amine (6069-38-1) + Cyclohex-2-enol (822-67-3) → N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ5-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide (699023-41-1)

Guidance literature:

(1,3-dimethyl-[1,3,2]diazaphospholidin-2-yl)-dimethyl-amine; Cyclohex-2-enol; In benzene; at 20 ℃; for 6h;

4-toluenesulfonyl azide; In benzene; at 20 ℃; for 0.25h;

DOI:10.1021/ja054161k

Reference yield:

Cyclohex-2-enol (822-67-3) → N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ5-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide (699023-41-1)

Guidance literature:

Multi-step reaction with 2 steps

1: benzene / 6 h / 20 °C

2: benzene / 0.25 h

In benzene;

DOI:10.1002/anie.200353284

Reference yield:

4-toluenesulfonyl azide (941-55-9) + 2-(cyclohex-2-enyloxy)-1,3-dimethyl-[1,3,2]diazaphospholidine → N-[2-(cyclohex-2-enyloxy)-1,3-dimethyl-2λ5-[1,3,2]diazaphospholidin-2-ylidene]-4-methyl-benzenesulfonamide (699023-41-1)

Guidance literature:

In benzene; for 0.25h;

DOI:10.1002/anie.200353284

upstream raw materials:

4-toluenesulfonyl azide

(1,3-dimethyl-[1,3,2]diazaphospholidin-2-yl)-dimethyl-amine

Cyclohex-2-enol

Downstream raw materials:

N-cyclohex-2-enyl-4-methyl-benzenesulfonamide

N-(cyclohex-2-enyl)-N-(1,3-dimethyl-2-oxo-2λ⁵-[1,3,2]diazaphospholidin-2-yl)-4-methylbenzenesulfonamide

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