N-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-4-methyl-benzenesulfonamide

Base Information

Chemical Name:N-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-4-methyl-benzenesulfonamide
CAS No.:272788-16-6
Molecular Formula:C₂₂H₂₉NO₄S
Molecular Weight:403.543
Hs Code.:

Synonyms:N-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-4-methyl-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-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-4-methyl-benzenesulfonamide

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Technology Process of N-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-4-methyl-benzenesulfonamide

There total 1 articles about N-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-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: 90.0%

: 70-55-3
toluene-4-sulfonamide

: 18522-92-4
sodium p-toluenesulfonamide

: (2S,3S)-2-Benzyloxymethyl-3-((Z)-pent-1-enyl)-oxirane

: 272788-16-6
N-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-4-methyl-benzenesulfonamide

Guidance literature:: tetrakis(triphenylphosphine) palladium⁽⁰⁾; In acetonitrile; at 40 ℃; for 6h;
DOI:10.1016/S0040-4020(99)01105-9

Reference yield: 91.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 272788-16-6
N-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-4-methyl-benzenesulfonamide

: 272788-18-8
N-[5-benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-1-propyl-pent-2-enyl]-4-methyl-benzenesulfonamide

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 4h;
DOI:10.1016/S0040-4020(99)01105-9

Reference yield:

: 272788-16-6
N-((E)-(1R,4R)-5-Benzyloxy-4-hydroxy-1-propyl-pent-2-enyl)-4-methyl-benzenesulfonamide

: 272788-21-3
(2S,5S)-5-(tert-Butyl-dimethyl-silanyloxy)-2-propyl-1-(toluene-4-sulfonyl)-piperidine

Guidance literature:: Multi-step reaction with 5 steps

1: 91 percent / imidazole / dimethylformamide / 4 h / 0 - 20 °C

2: 97 percent / H₂ / PtO₂ / ethanol / 3 h / 20 °C / 760 Torr

3: 93 percent / H₂ / Pd/C / methanol / 1 h / 20 °C / 760 Torr

4: Et₃N / tetrahydrofuran / 3 h / 0 - 20 °C

5: 81 percent / K₂CO₃ / methanol / 23 h / 20 °C

With 1H-imidazole; hydrogen; potassium carbonate; triethylamine; platinum(IV) oxide; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; 1: Addition / 2: Hydrogenation / 3: Hydrogenation / 4: Addition / 5: Cyclization;
DOI:10.1016/S0040-4020(99)01105-9