(2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate

Base Information

Chemical Name:(2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate
CAS No.:571153-37-2
Molecular Formula:C₃₂H₃₁Cl₂N₃O₄Se
Molecular Weight:671.482
Hs Code.:

Synonyms:(2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate

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Chemical Property of (2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate

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Technology Process of (2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate

There total 4 articles about (2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate 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: 87.0%

: 5707-04-0
Phenylselenyl chloride

: 455262-36-9
ethyl (2S)-2-[(3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propanoate

: 571153-37-2
(2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate

Guidance literature:: In tetrahydrofuran; dichloromethane; at 20 ℃;
DOI:10.1021/ol034701n

Reference yield:

: 2719-27-9
cyclohexanylcarbonyl chloride

: 571153-37-2
(2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate

Guidance literature:: Multi-step reaction with 4 steps

1: 81 percent / triethylamine / diethyl ether; hexane / 24 h / Heating

2: 92 percent / hydrochloric acid / H₂O / 24 h / 20 °C

3: 95 percent / tetrahydrofuran / 24 h / 20 °C

4: 87 percent / tetrahydrofuran; CH₂Cl₂ / 20 °C

With hydrogenchloride; triethylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water;
DOI:10.1021/ol034701n

Reference yield:

: 10576-21-3
3-ethoxyspiro[3.5]non-2-en-1-one

: 571153-37-2
(2S)-ethyl 2-[(2-phenylselenenyl-3-oxospiro[3.5]non-1-en-1-yl)amino]-3-{4-[(3,5-dichloroisonicotinoyl)amino]phenyl}propionate

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / hydrochloric acid / H₂O / 24 h / 20 °C

2: 95 percent / tetrahydrofuran / 24 h / 20 °C

3: 87 percent / tetrahydrofuran; CH₂Cl₂ / 20 °C

With hydrogenchloride; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/ol034701n