N-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-benzenesulfonamide

Base Information

Chemical Name:N-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-benzenesulfonamide
CAS No.:466645-81-8
Molecular Formula:C₂₅H₃₉N₃O₅SSi
Molecular Weight:521.753
Hs Code.:

<i>N</i>-allyl-<i>N</i>-[4-allylamino-6-(<i>tert</i>-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-benzenesulfonamide

Synonyms:N-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-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-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-benzenesulfonamide

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Technology Process of N-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-benzenesulfonamide

There total 5 articles about N-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-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: 86.0%

: 107-11-9,30551-89-4
1-amino-2-propene

: 466645-80-7
N-allyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-chloro-cyclohept-2-enyl]-4-nitro-benzenesulfonamide

: 466645-81-8
N-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-benzenesulfonamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 70 ℃; for 18h;
DOI:10.1021/jo025666l

Reference yield:

: 100704-44-7
N-allyl-p-nitrobenzenesulfonamide

: 466645-81-8
N-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / diisopropylazodicarboxylate; PPh₃ / tetrahydrofuran / 18 h / 20 °C

2: 95 percent / KCN / methanol / 18 h / 20 °C

3: 85 percent / mesyl chloride; pyridine / 18 h / 20 °C

4: 86 percent / K₂CO₃ / acetonitrile / 18 h / 70 °C

With pyridine; potassium cyanide; di-isopropyl azodicarboxylate; potassium carbonate; methanesulfonyl chloride; triphenylphosphine; In tetrahydrofuran; methanol; acetonitrile; 1: Mitsunobu reaction;
DOI:10.1021/jo025666l

Reference yield:

: 134734-52-4
(1R,4S,6S)-4-acetoxy-6-[(tert-butyldimethylsilyl)oxy]-2-cyclohepten-1-ol

: 466645-81-8
N-allyl-N-[4-allylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-4-nitro-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / diisopropylazodicarboxylate; PPh₃ / tetrahydrofuran / 18 h / 20 °C

2: 95 percent / KCN / methanol / 18 h / 20 °C

3: 85 percent / mesyl chloride; pyridine / 18 h / 20 °C

4: 86 percent / K₂CO₃ / acetonitrile / 18 h / 70 °C

With pyridine; potassium cyanide; di-isopropyl azodicarboxylate; potassium carbonate; methanesulfonyl chloride; triphenylphosphine; In tetrahydrofuran; methanol; acetonitrile; 1: Mitsunobu reaction;
DOI:10.1021/jo025666l