N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Base Information

Chemical Name:N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide
CAS No.:482376-70-5
Molecular Formula:C₂₇H₄₃N₃O₅SSi
Molecular Weight:549.807
Hs Code.:

<i>N</i>-but-3-enyl-<i>N</i>-[4-but-3-enylamino-6-(<i>tert</i>-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Synonyms:N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

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Chemical Property of N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

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Technology Process of N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

There total 5 articles about N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-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%

: 2524-49-4
3-butene-1-amine

: 482376-68-1
N-but-3-enyl-N-[6-(tert-butyl-dimethyl-silanyloxy)-4-chloro-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

: 482376-70-5
N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 70 ℃; for 18h;
DOI:10.1002/1099-0690(200208)2002:16<2855::AID-EJOC2855>3.0.CO;2-1

Reference yield:

: 90870-33-0
N-(2-nitrobenzenesulfonyl)-N-(but-3-enyl)amine

: 482376-70-5
N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / EtOOC-N=N-COOEt; Ph₃P / tetrahydrofuran / 18 h / 20 °C

2: 96 percent / KCN; MeOH / 15 h / 20 °C

3: 82 percent / MsCl; pyridine / 18 h / 20 °C

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

With pyridine; methanol; potassium cyanide; potassium carbonate; methanesulfonyl chloride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; acetonitrile; 1: Mitsunobu reaction;
DOI:10.1002/1099-0690(200208)2002:16<2855::AID-EJOC2855>3.0.CO;2-1

Reference yield:

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

: 482376-70-5
N-but-3-enyl-N-[4-but-3-enylamino-6-(tert-butyl-dimethyl-silanyloxy)-cyclohept-2-enyl]-2-nitro-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / EtOOC-N=N-COOEt; Ph₃P / tetrahydrofuran / 18 h / 20 °C

2: 96 percent / KCN; MeOH / 15 h / 20 °C

3: 82 percent / MsCl; pyridine / 18 h / 20 °C

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

With pyridine; methanol; potassium cyanide; potassium carbonate; methanesulfonyl chloride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; acetonitrile; 1: Mitsunobu reaction;
DOI:10.1002/1099-0690(200208)2002:16<2855::AID-EJOC2855>3.0.CO;2-1