Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester

Base Information

Chemical Name:Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester
CAS No.:1027914-27-7
Molecular Formula:C₁₈H₂₂N₂O₆S
Molecular Weight:394.448
Hs Code.:

Synonyms:Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester

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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 Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester

Chemical Property:

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Technology Process of Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester

There total 1 articles about Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester 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: 88.0%

: 65118-17-4
N-allyl-o-nitrobenzenesulfonamide

: 121961-66-8,606490-58-8
(1R,4S)-4-hydroxycyclohept-2-enyl acetate

: 1027914-27-7
Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/S0040-4039(02)01534-4

Reference yield: 84.0%

: 501-53-1,94274-21-2
benzyl chloroformate

: 1027914-27-7
Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester

: Acetic acid (1R,4R)-4-(allyl-benzyloxycarbonyl-amino)-cyclohept-2-enyl ester

Guidance literature:: Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester; With potassium carbonate; thiophenol; In N,N-dimethyl-formamide; at 70 ℃;

benzyl chloroformate; In N,N-dimethyl-formamide; at 0 ℃;
DOI:10.1016/S0040-4039(02)01534-4

Reference yield:

: 1027914-27-7
Acetic acid (1R,4R)-4-[allyl-(2-nitro-benzenesulfonyl)-amino]-cyclohept-2-enyl ester

: Allyl-((1R,4R)-4-hydroxy-cyclohept-2-enyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate; thiophenol / N,N-dimethyl-formamide / 70 °C

1.2: 27 / 0 °C

2.1: methanol; sodium cyanide / 20 °C

With methanol; sodium cyanide; potassium carbonate; thiophenol; In N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(02)01534-4