N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

Base Information

Chemical Name:N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide
CAS No.:300363-47-7
Molecular Formula:C₂₅H₃₂N₂O₄S
Molecular Weight:456.606
Hs Code.:

<i>N</i>-(1-benzyloxymethyl-allyl)-4-methyl-<i>N</i>-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

Synonyms:N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

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Technology Process of N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

There total 5 articles about N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-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: 85.0%

: 100-39-0
benzyl bromide

: 300363-46-6
N-(1-hydroxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

: 300363-47-7
N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran;
DOI:10.1016/S0957-4166(00)00237-8

Reference yield:

: 300363-42-2
3-[1-(tert-butyl-diphenyl-silanyloxymethyl)-allylamino]-propionic acid methyl ester

: 300363-47-7
N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / Et₃N / CH₂Cl₂ / 0 - 20 °C

2: 86 percent / aq. LiOH / acetone

3: 80 percent / BOPCl; DMAP / CH₂Cl₂

4: 98 percent / TBAF / tetrahydrofuran

5: 85 percent / NaH; TBAI / tetrahydrofuran

With dmap; lithium hydroxide; tetrabutyl ammonium fluoride; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane; acetone; 1: Tosylation / 2: Hydrolysis / 3: Acylation / 4: desilylation / 5: Etherification;
DOI:10.1016/S0957-4166(00)00237-8

Reference yield:

: 300363-43-3
3-[[1-(tert-butyl-diphenyl-silanyloxymethyl)-allyl]-(toluene-4-sulfonyl)-amino]-propionic acid methyl ester

: 300363-47-7
N-(1-benzyloxymethyl-allyl)-4-methyl-N-(3-oxo-3-pyrrolidin-1-yl-propyl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 86 percent / aq. LiOH / acetone

2: 80 percent / BOPCl; DMAP / CH₂Cl₂

3: 98 percent / TBAF / tetrahydrofuran

4: 85 percent / NaH; TBAI / tetrahydrofuran

With dmap; lithium hydroxide; tetrabutyl ammonium fluoride; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; dichloromethane; acetone; 1: Hydrolysis / 2: Acylation / 3: desilylation / 4: Etherification;
DOI:10.1016/S0957-4166(00)00237-8